Patent Application
20150080613
This invention relates to a method for preparing glycerol ether and glycol ether.
Glycerol and its derivatives are significant industrial by-products, in particular in the biodiesel fuel industry. It is therefore particularly beneficial to find new ways to upgrade these products.
Glycerol ethers and glycol ethers can be used in numerous fields, such as cosmetics, detergents, washing formulations and in the pharmaceutical field. These ethers can constitute a new line of particularly beneficial surfactants since they are obtained from biosourced materials. However, there are few synthesis methods enabling these ethers to be obtained in a simple and inexpensive manner.
From JP 200-119205 in particular, a method for producing glycerol ether from glycerol carbonate by reaction in the presence of a base (in particular KOH) is known. However, the use of this method does not enable a good glycerol ether yield to be obtained; indeed, the transcarbonation compound is primarily formed.
The objective of this invention is to provide a method for selective preparation of glycerol ether or derivatives of glycerol and glycol ether.
Another objective of this invention is to provide such a method that makes it possible to obtain, with good yields, the desired ether.
Another objective of this invention is to provide a method for preparing surfactants from biosourced compounds.
Another objective is to provide a continuous method for preparing glycerol ether or derivatives of glycerol and glycol ether.
This invention relates to a method for preparing glycerol ether or glycol ether of formula (I) and/or (I′), comprising the reaction of a compound of formula (II) with a compound of formula (III) in the presence of a heterogeneous acid catalyst
wherein
R1 is a hydrogen atom or an alkyl radical, linear or branched, comprising 1 to 15 carbon atoms, preferably 1 to 10 carbon atoms;
R2 is a hydrogen atom; an alkyl radical, linear or branched, comprising 1 to 15 carbon atoms, preferably 1 to 10 carbon atoms; or a group of formula —(CH2)nOH, wherein n is an integer between 0 and 5, and n is preferably equal to 0 or 1;
R3 is an alkyl radical, linear or branched, capable of comprising one or more unsaturations, comprising 1 to 40 carbon atoms, and optionally capable of comprising 1 or more hydroxy substituents (OH).
In the context of the invention, it is possible to selectively obtain one of compounds (I) or (I′) or a mixture of these two compounds according to the definition of the R1 and R2 groups, the steric hindrance orienting the reaction toward the addition of the OR3 group on the less hindered side. Thus, without being bound to any one theory, preferably:
Preferably, in the method of the invention R1 is a hydrogen atom, R2 is —CH2OH, compound (II) thus preferred is glycerol carbonate, and the compound formed is a compound of formula (I):
Preferably, in the method of the invention, R3 is an alkyl radical, linear or branched, optionally comprising one or more unsaturations, comprising 1 to 40 carbon atoms. In a preferred embodiment, R3 is an alkyl radical, linear or branched, optionally comprising one or more unsaturations, comprising 12 to 40 carbon atoms, preferably 24 to 30 carbon atoms. In another preferred embodiment R3 is an alkyl radical, linear or branched, optionally comprising one or more unsaturations, comprising 1 to 15 carbon atoms.
In one embodiment, the method relates to the preparation of glycerol ether.
In another embodiment, the method relates to the preparation of glycol ether.
The features described below apply to each of these two embodiments.
Advantageously, the heterogeneous acid catalyst of the invention has an acid site concentration greater than or equal to 0.01 mequi/g (or mEq/g or me/g) (milliequivalent of H+ ions per gram) of catalyst, preferably 0.01 to 10 mequi/g (or mEq/g or me/g), more preferably 0.01 to 6 mequi/g (or mEq/g or me/g), preferably 0.01 to 5 mequi/g (or mEq/g or me/g). This makes it possible in particular to obtain a good conversion of the compound of formula (II) and a good ether yield (compound of formula (I) or (I′)). Advantageously, the greater the acid site concentration is, the higher the glycerol ether yield will be.
In the context of this invention, the term “acid site concentration” refers to the surface acidity due to H+ protons at the surface of the catalyst. This acid site concentration is determined by any method known to a person skilled in the art, and in particular usually by determining the milliequivalent number of H− protons brought to 1 g of catalyst (mequi/g (mEq/g or me/g) of catalyst). The acid site concentration in mEq/g corresponds to the ion exchange capacity of the catalyst expressed in mEq of H− per gram of catalyst.
Advantageously, the heterogeneous catalyst according to the invention has a specific surface measured by the BET method of 5 to 500 m2/g, preferably 10 to 100 m2/g. The specific surface is determined by the BET method, for example by the nitrogen adsorption and desorption method.
This makes it possible in particular to obtain a good conversion of the compound of formula (II) and a good ether yield. Advantageously, the greater the specific surface is, the higher the glycerol ether or glycol ether yield will be.
Preferably, the heterogeneous catalyst according to the invention is characterized by a Hammett constant (Ho) of −3 to −12, preferably −5 to −12. This makes it possible, in particular, to obtain a good conversion of the compound of formula (II) and a good ether yield. Advantageously, the lower the Ho is, the higher the glycerol ether or glycol ether yield will be.
The Hammett constant can be determined by any method known to a person skilled in the art and is in particular determined by a standardized colorimetric method called the Tanabe method (TANABE et al. The Journal of Physical Chemistry, (1976) 15, 1723).
The acid catalyst AH is reacted with a colour indicator B, the reaction leads to the formation of A− and BH+. The Ho value is then determined by the formula (A):
In this formula, pKa(BH+/B) is the pKa of the acid/base pair (BH+/B); [B] is the concentration of B and [BH−] is the concentration of BH−.
Preferably, the catalyst is chosen from the group consisting of the acid forms of ion exchange resins; supports impregnated with sulphuric acid, hydrochloric acid, niobic acid, hydrofluoric acid, antimony pentafluoride, heteropoly acids, triflic acid, or sulfonic or phosphoric acid; sulphated zirconia; zeolites, in particular aluminosilicate zeolite, for example zeolite Y characterized by a faujasite structure; and mixed oxides, in particular TiO2/Al2O3, ReO7/Al2O3, TiO2/ZrO2, SiO2/Al2O3.
The supports are in particular chosen from metal oxides, in particular Al2O3, ZrO2, TiO2; SiO2; or carbons.
In an especially preferred manner, the catalyst is chosen from the acid forms of ion exchange resins; supports impregnated with sulphuric acid or sulfonic acid; and sulphated zirconia.
Even more preferably, the heterogeneous catalyst is chosen from the acid forms of ion exchange resins.
All of the preferred or advantageous features of the acid catalyst according to the invention can be combined with one another.
The ion exchange acid resins can in particular be chosen from the ion exchange acid resins bearing sulfonic groups. They may in particular be chosen from the resins consisting of a polystyrene skeleton bearing sulfonic groups or from the perfluorinated resins bearing sulfonic groups.
Preferably, the resins consisting of a polystyrene skeleton are styrene-divinylbenzene copolymers comprising sulfonic groups. Such a resin is obtained by polymerization of the styrene and the divinylbenzene under the influence of an activation catalyst, usually in suspension. Beads or granules are obtained, which are then treated with concentrated sulphuric or chlorosulphuric acid. The proportion of the sulfonic groups with respect to the polymeric mass can be variable, and will be taken into account when determining the amount of polymer to use. Such resins are in particular commercially available under the name Amberlyst® (sold by the Dow company). Preferably, these resins are chosen from Amberlyst® 35, Amberlyst® 36, Amberlyst® 70 or Amberlyst® 21.
Preferably, the perfluorinated resins bearing sulfonic groups are tetrafluoroethylene and perfluoro[2-(fluorosulfonyl-ethoxy)-propyl]vinyl ether copolymers, in particular those sold under the name Naflon®. These resins have the following formula:
wherein m is an integer with a value of 1, 2 or 3, n is an integer from 5 to 13 and x is generally around 1000.
Particularly preferably, the resins are resins consisting of a polystyrene skeleton bearing sulfonic groups.
Preferably, the catalyst is used in proportions of 2% to 40%, preferably 5% to 20% by weight with respect to the weight of the compound of formula (II).
Preferably, the molar ratio of formula (II) compound/formula (III) compound is 1/1 to 1/5, and preferably 1/2 to 1/4.
It is preferable, in the context of the method of the invention, to control the amount of water introduced by the different reagents. It is thus preferable to dry the reagents before use.
The maximum temperature used in the method of the invention is primarily dependent upon the acid used. In fact, certain resins are sensitive to temperature. A person skilled in the art can therefore adapt the temperature of the method to the acid used. Preferably, the method of the invention can be implemented at a temperature of 100° C. to 200° C., preferably 100° C. to 170° C., for example 100° C. to 150° C.
The duration of the method of this invention can be 30 minutes to 24 hours, and preferably 30 minutes to 12 hours.
The method of the invention can be performed in batch or continuous mode, and is preferably performed in continuous mode.
The method of the invention advantageously makes it possible to obtain glycerol ethers with a purity greater than or equal to 90%, preferably greater than or equal to 99%.
Particularly advantageously, when the compound of formula (III) is a fatty alcohol, i.e. when R3 is an alkyl, linear or branched, comprising 12 to 40 carbon atoms, preferably 24 to 30 carbon atoms, the ethers thus obtained may in particular be used as surfactants. These ethers will in particular advantageously be capable of being used as surfactants in detergent compositions, cosmetic compositions, washing formulations and in the pharmaceutical field.
According to the invention, the method may comprise a preliminary step of preparing the compound of formula (II). This preliminary step is performed by a reaction between a compound of formula (IV) and carbon dioxide, in the presence of a lanthanide-based catalyst:
wherein R1 and R2 are as defined for formula (I).
In one embodiment, the lanthanide-based catalyst is chosen from the lanthanide family, and more specifically from the rare earth group, supported or unsupported.
The term “rare earth” (designated throughout the description by the generic term Ln) refers to chemical elements chosen from the group consisting of cerium (Ce), lanthanum (La), praseodymium (Pr), neodymium (Nd), yttrium (Y), gadolinium (Gd), samarium (Sm) and holmium (Ho), alone or in a mixture, preferably cerium, lanthanum, praseodymium and neodymium, alone or in a mixture.
In one embodiment, the catalyst is chosen from the group consisting of lanthanide oxides of formula Ln2O3 (for lanthanum, neodymium, yttrium, gadolinium, samarium and holmium) or CeO2 or Pr6O11, lanthanide carbonates of formula Ln2(CO3)3, lanthanide hydroxycarbonates of formula Ln(OH)(CO3), lanthanide oxycarbonates of formula Ln2O(CO3)2 and lanthanide hydroxides of formula Ln(OH)3, alone or in a mixture.
In a preferred embodiment, the catalyst is chosen from the group consisting of lanthanide oxides, lanthanide carbonates and lanthanide hydroxycarbonates, alone or in a mixture; preferably, the catalyst is chosen from the group consisting of lanthanide oxides, or lanthanide carbonates, alone or in a mixture.
In one embodiment, the catalyst is a rare earth oxide.
In one embodiment, the catalyst of the preliminary step is chosen from the group consisting of CeO2 and Pr6O11.
In one embodiment, the catalyst of the preliminary step is in oxide form and has a specific surface of at least 5 m2/g, preferably at least 10 m2/g, and more preferably at least 30 m2/g.
In one embodiment of the invention, the catalyst of the preliminary step, as defined above, is doped by Lewis acid-type metals, for example transition metals, alkaline earth metals and metalloids.
In one embodiment, these metals are chosen from the group consisting of iron (Fe(II) and Fe(III)), copper (Cu(I) and Cu(III)), aluminium (Al(III)), titanium (Ti(IV)), boron (B(III)), zinc (Zn(II)) and magnesium (Mg(II)).
Preferably, these metals are chosen from the group consisting of iron (Fe(II) and Fe(III)), copper (Cu(I) and Cu(III)), titanium (Ti(IV)) and zinc (Zn(II)).
In one embodiment, the catalyst is a rare earth oxide modified with transition metals.
In this embodiment, the relative percentage of metals with respect to the lanthanide material is between 1 and 10% by weight, and preferably between 1 and 5% by weight.
In one embodiment of the invention, in order to minimize costs, the catalyst may be a mixed system based on rare earths and other minerals such as ZnO, MgO, Al2O3 or SiO2.
This particular embodiment makes it possible to provide additional properties in terms of both the acid-basic properties and the mechanical properties of the catalysts.
Advantageously, the molar ratio between the compound of formula (IV) and CO2 is between 1 and 150 molar equivalents, preferably between 1 and 100 equivalents.
According to the invention, the preliminary step of preparing the compound of formula (II) is implemented at autogenous pressure or at atmospheric pressure.
According to the invention, the preliminary step of preparing the compound of formula (II) is implemented at a temperature of between 25 and 250° C., preferably between 25 and 200° C., for example between 50 and 150° C.
Advantageously, the amount of catalyst is between 0.01 and 50% by weight with respect to the weight of the compound of formula (IV), preferably between 1 and 25% by weight, and preferably between 3 and 15% by weight.
This invention will now be described with the assistance of non-limiting examples.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 5.20 g (40 mmol) of commercial n-octanol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 118 mg (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2 as well as 5 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is then purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give glycerol 1-O-octylether with an isolated yield of 45%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 6.33 g (40 mmol) of commercial n-decanol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 118 mg (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2 as well as 5 mL of H2O are added. The organic phase is then decanted.
The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is then purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give glycerol 1-O-decylether with an isolated yield of 46%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 7.44 g (40 mmol) of commercial n-dodecanol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 118 mg (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2 as well as 5 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is then purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give glycerol 1-O-dodecylether with an isolated yield of 40%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 5.20 g (40 mmol) of commercial n-octanol and 118 mg of Amberlyst A 36 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 118 mg (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2 as well as 5 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is analysed without purification by gas phase chromatography. Glycerol octyl ether is detected with a GC yield of 15%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 5.20 g (40 mmol) of commercial n-octanol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 1.02 g (10 mmol) of propylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2 as well as 5 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is analysed without purification by gas phase chromatography. Octyl propylene glycol ether is detected with a GC yield of 85% for a conversion of 90%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 3.53 g (40 mmol) of commercial pentan-1-ol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 1.18 g (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give glycerol 1-O-pentyl ether with an isolated yield of 49%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 4.65 g (40 mmol) of commercial heptan-1-ol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 1.18 g (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give glycerol 1-O-heptyl ether with an isolated yield of 42%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 8.57 g (40 mmol) commercial tetradecanol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 1.18 g (10 mmol) of glycerol carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2, as well as 5 mL d′H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give glycerol 1-O-tetradecylether with an isolated yield of 45%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 3.52 g (40 mmol) of commercial pentan-1-ol and 88 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 0.88 g (10 mmol) of ethylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 0/1 to 1/10)) to give ethylene glycol 1-O-pentyl ether with an isolated yield of 46%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 4.65 g (40 mmol) of commercial heptan-1-ol and 88 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 0.88 g (10 mmol) of ethylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 0/1 to 1/10)) to give ethylene glycol 1-O-heptyl ether with an isolated yield of 43%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 5.21 g (40 mmol) of commercial octan-1-ol and 88 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 0.88 g (10 mmol) of ethylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 0/1 to 1/10)) to give ethylene glycol 1-O-octyl ether with an isolated yield of 42%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 6.33 g (40 mmol) of commercial decanol and 88 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 0.88 g (10 mmol) of ethylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 0/1 to 1/10)) to give ethylene glycol 1-O-decyl ether with an isolated yield of 37%.
In a 25-mL three-necked flask, provided with a coolant and a nitrogen inlet, 7.45 g (40 mmol) of commercial dodecan-1-ol and 88 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 0.88 g (10 mmol) of ethylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 10 mL of CH2Cl2, as well as 2 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×10 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 0/1 to 1/10)) to give ethylene glycol 1-O-dodecyl ether with an isolated yield of 28%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 3.52 g (40 mmol) of commercial pentan-1-ol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 118 mg (10 mmol) of propylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2, as well as 5 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give propylene glycol 1-O-pentyl ether with an isolated yield of 42%.
In a 50-mL three-necked flask, provided with a coolant and a nitrogen inlet, 4.65 g (40 mmol) of commercial heptan-1-ol and 118 mg of Amberlyst A 35 solid acid are introduced at room temperature. The reaction medium is then brought to 140° C. and 118 mg (10 mmol) of propylene carbonate are added over a period of one hour. The heating at 140° C. is then extended for 1 h after the end of the addition. Then, the reaction medium is brought to room temperature. Then, 20 mL of CH2Cl2, as well as 5 mL of H2O are added. The organic phase is then decanted. The aqueous phase is extracted by 2×25 mL of CH2Cl2. The organic phases are combined and the CH2Cl2 is evaporated under reduced pressure. The crude reaction product is finally purified by flash silica column chromatography (Eluent (AcOEt/cyclohexane: 1/4 to 1/1)) to give propylene glycol heptyl ether with an isolated yield of 40%.
The following table presents the results of the different tests performed.
These results show that the method according to the invention enables a good conversion of glycerol carbonate and the formation of glycerol ether to be obtained.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1252624 | Mar 2012 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2013/056280 | 3/25/2013 | WO | 00 |
