Claims
- 1. A method for preparing a sulfonated ester of the formula:
- RO(CH.sub.2 CHR.sub.1 O).sub.n COCH.sub.2 SO.sub.3 M
- where
- R represents straight chain alkyl having from about 6 to 22 carbon atoms;
- R.sub.1 is hydrogen, methyl, or ethyl;
- n is 0, or an integer of from 1 to 22; and
- M represents Ca.sup.++, Mg.sup.++, Na.sup.+, K.sup.+ or NH.sub.4.sup.+ ;
- comprising reacting an alkyl chloroester of the formula RO(CH.sub.2 CHR.sub.1 O).sub.n COCH.sub.2 Cl where R, R.sub.1 and n are defined as above with at least about a 3% molar excess of an aqueous sulfite in the presence of from about 0.1 to 5% by weight of reactants of a sulfitation catalyst at a temperature of at least about 75.degree. C.
- 2. A method for preparing a sulfonated ester according to claim 1, where the sulfitation catalyst is selected from the group consisting of iodide containing species, metallic copper and alkyl sulfoacetates.
- 3. A method for preparing a sulfonated ester according to claim 2, wherein the iodide containing species is selected from the group consisting of the iodides of sodium, potassium, lithium, calcium, copper, aluminum, manganese, tin, and phosphorous.
- 4. A method according to claim 2, wherein the molar excess is about a 15 to 50% molar excess.
- 5. A method according to claim 4, wherein the molar excess is about a 33% molar excess.
- 6. A method according to claim 5, wherein the temperature of the reaction is about 85.degree.-99.degree. C.
- 7. A method according to claim 6, wherein the amount of the catalyst is from about 0.5 to 2% based on the weight of reactants.
- 8. A method according to claim 1, where the sulfitation catalyst is an alkyl sulfoacetate comprising a monochloroacetate selected from the group consisting of monochloroacetic acid, alkali metal monochloroacetates, and mixtures thereof, the alkyl sulfoacetate being present in the reaction in an amount of about 0.1 to 5% based on the weight of reactants.
- 9. A method for preparing a sulfonated ester according to claim 1, further comprising the step of drying the sulfonated ester.
- 10. A method for preparing a sulfonated ester according to claim 1, further comprising the step of bleaching the sulfonated ester.
- 11. In a method for preparing an alkyl sulfoacetate of the formula:
- RO(CH.sub.2 CHR.sub.1 O).sub.n COCH.sub.2 SO.sub.3 M
- where
- R represents straight chain alkyl having from about 6 to 22 carbon atoms;
- R.sub.1 is hydrogen, methyl, or ethyl;
- n is 0, or an integer of from 1 to 22; and
- M represents Ca.sup.++, Mg.sup.++, Na.sup.+, K.sup.+ or NH.sub.4.sup.30 ,
- in which an alkyl chloroester of the formula ROCOCH.sub.2 Cl where R is defined as above is reacted with sodium sulfite, the improvement comprising reacting the alkyl chloroester with at least about a 33% molar excess of aqueous sodium sulfite in the presence of at least about 0.1% by weight of reactants of a sulfitation catalyst at a temperature of from about 75.degree.-105.degree. C., the alkyl sulfoacetate having less than about 5 ppm of sodium monochloroacetate and less than about 5 ppm of monochloroacetic acid, the amounts of monochloroacetic acid and monochloroacetate being based on the total weight of solids.
- 12. A method for preparing a sulfonated ester according to claim 11, wherein the iodide containing species is selected from the group consisting of the iodides of sodium, potassium, lithium, calcium, copper, aluminum, manganese, tin, and phosphorous.
- 13. A method according to claim 12, where the sulfitation catalyst is an alkyl sulfoacetate comprising from about 0-10% by weight of monochloroacetate based on the weight of alkyl sulfoacetate, the alkyl sulfoacetate being present in the reaction in an amount of about 0.1 to 5% based on the weight of reactants.
- 14. A method according to claim 11, wherein the molar excess is about a 15 to 50% molar excess.
- 15. A method according to claim 11, wherein the temperature of the reaction is from about 85.degree.to 99.degree. C.
Parent Case Info
This is a continuation of application Ser. No. 08/259,462, filed Jun. 14, 1994 abandoned on Nov. 17, 1995.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
4807649 |
Eoga |
Feb 1989 |
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Continuations (1)
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Number |
Date |
Country |
Parent |
259462 |
Jun 1994 |
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