Patent Application
20170297984
The present invention relates to a catalytic process for the ethynylation of specific poly-unsaturated aldehydes and ketones.
Polyunsaturated aldehydes and ketones in the context of the present invention are aldehydes and ketones wherein the aldehydes and ketones comprise at least two C—C double bonds. In some embodiments of the present invention the C═C double bonds can also be conjugated.
Polyunsaturated aldehydes and ketones (with conjugated C═C double bonds), such as the α,β-unsaturated ones, are quite stable compounds.
The reaction products, which are the outcome of the process according to the present invention are useful intermediates in the production of important organic compounds (such as for example vitamin A or carotenoids).
Known ethynylations of specific polyunsaturated aldehydes and ketones are stoichiometric processes, such as for example the Grignard reaction. This very well-known reaction produces—due to the need of stoichiometric amounts—a significant amount of waste material at the end of the process. Also the chemical compounds which are used in such processes are not easy to handle.
Now the goal was to find an improved process for the ethynylation of the specific polyunsaturated aldehydes and ketones, which are represented by the following formula (I)
wherein
R1 signifies —H, —CH3 or —CH2CH3, and
R2 signifies —H, —CH3 or —CH2CH3, and
R3 signifies a moiety
Surprisingly it was found that these specific (at least α,-β, unsaturated) polyunsaturated aldehydes and ketones can be ethynylated catalytically.
The ethynylation is carried out with ethyne (=acetylene; HCCH) under pressure by using at least one solvent and at least one catalyst.
wherein
R1, R2, R3 are as defined above and
R is K or Cs, preferably K.
Therefore, the present invention relates to a catalytic ethynylation (CE) of compounds of formula (I)
wherein
R1 signifies —H, —CH3 or —CH2CH3, and
R2 signifies —H, —CH3 or —CH2CH3, and
R3 signifies a moiety
with ethyne
in the presence of a catalyst of formula ROH wherein
R signifies K or Cs, and wherein
NH3 is used as solvent.
As stated above, the catalytic ethynylation of such important specific compounds of formula (I) are not known from the prior art.
This new method is an alternative way to for ethynylation, with significant advantages a catalytic process has (less starting material, less waste, safety of the process etc).
Preferred is a catalytic ethynylation as described above wherein formula (I)
R1 signifies —H or —CH3
R2 signifies —H or —CH3.
Therefore, the present invention relates to a catalytic ethynylation (CE1), which is ethynylation (CE), wherein formula (I)
R1 signifies —H or —CH3
R2 signifies —H or —CH3, preferably —H.
More preferred is the catalytic ethynylation of a compound of formula (Ia)
The corresponding ethynylated compound is the one of formula (IIa)
More preferred is the catalytic ethynylation of a compound of formula (Ib)
The corresponding ethynylated compound is the one of formula (IIb)
More preferred is the catalytic ethynylation of a compound of formula (Ic)
The corresponding ethynylated compound is the one of formula (IIc):
Therefore, the present invention also relates to a catalytic ethynylation (CE2), which is ethynylation (CE), wherein the compound of formula (I) is the compound of formula (Ia)
Therefore, the present invention also relates to a catalytic ethynylation (CE3), which is ethynylation (CE), wherein the compound of formula (I) is the compound of formula (Ib)
Therefore, the present invention also relates to a catalytic ethynylation (CE4), which is ethynylation (CE), wherein the compound of formula (I) is the compound of formula (Ic)
The catalyst (KOH or CsOH as well as mixture of these compounds) is usually added to the reaction mixture as an aqueous solution (30-60 wt-%, preferably 40-50 wt-%, based on the total weight of the aqueous catalyst solution).
It is preferred that the catalyst according to the present invention is KOH (R is K).
Therefore, the present invention also relates to a catalytic ethynylation (CE5), which is ethynylation (CE), (CE1), (CE2), (CE3) or (CE4), wherein R is K.
Therefore, the present invention also relates to a catalytic ethynylation (CE6), which is ethynylation (CE), (CE1), (CE2), (CE3), (CE4) or (CE5), wherein the catalyst is added to the reaction mixture as an aqueous solution (30-60 wt-%, of the catalyst, preferably 40-50 wt-%, based on the total weight of the aqueous catalyst solution).
The catalytic ethynylation according to the present invention is usually carried out under pressure. The pressure is in the range from 2 bar to 15 bar, preferably from 5 bar to 12 bar, more preferably from 6 bar to 10 bar.
Therefore, the present invention also relates to a catalytic ethynylation (CE7), which is ethynylation (CE), (CE1), (CE2), (CE3), (CE4), (CE5) or (CE6), wherein the pressure is in the range from 2 bar to 15 bar (preferably from 5 bar to 12 bar, more preferably from 6 bar to 10 bar).
The catalytic ethynylation according to the present invention is usually carried at a reaction temperature of between −40° C.-10° C., preferably −30°-5° C.
Therefore, the present invention also relates to a catalytic ethynylation (CE8), which is ethynylation (CE), (CE1), (CE2), (CE3), (CE4), (CE5), (CE6) or (CE7), wherein the process is carried at a reaction temperature of between −40° C.-10° C. (preferably −30°-5° C.).
The obtained reaction products are useful intermediates in organic synthesis, for example in the production of vitamin A (or vitamin A acetate) or carotenoids.
The following Examples illustrate the invention further without limiting it. All percentages and parts, which are given, are related to the weight and the temperatures are given in ° C., when not otherwise stated.
The reaction was carried out in a 1 L-autoclave, which was washed with N2 before its use. Afterwards 150 g NH3 was added into the autoclave and cooled to −20° C. At this temperature acetylene (ethyne) was added so that the pressure was 5.6 bara. Afterwards 1.68 g of KOH (as a 44 wt-% solution in H2O) was added followed by 354.45 g of the compound of formula (Ic). After 4 h reaction time, the reaction mixture was diluted with 100 ml n-heptane.
The obtained product (compound of formula (IIc)
was purified and it was obtained in a yield of 32%.
The reaction was carried out in a 1 L-autoclave, which was washed with N2 before its use. Afterwards 150 ml of NH3 was added and cooled to −20° C. At this temperature acetylene (ethyne) was added so that the pressure was 5.6 bara. 1.68 g of KOH (as a 44 wt-% solution in H2O) was added.
Afterwards 5 g of the compound of formula (Ia), dissolved in 5 g toluene, was added. After 6 h reaction time, the reaction mixture was diluted with 100 ml toluene.
The obtained product (compound of formula (IIa)
was purified and it was obtained in a yield of 57%.
| Number | Date | Country | Kind |
|---|---|---|---|
| 14189262.0 | Oct 2014 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2015/073868 | 10/15/2015 | WO | 00 |
