Process for making secondary amphoacetates and diacetates

Details Process for making secondary amphoacetates and diacetates Process for making secondary amphoacetates and diacetates

1999-04-30

2000-02-15

Geist, Gary

Organic compounds -- part of the class 532-570 series

Organic compounds

Carboxylic acids and salts thereof

562564, C07C 5116, C07C22922, C07C22930

Patent

active

060255226

ABSTRACT:
Process for making secondary amphoacetate and amphodiacetate of the formula ##STR1## wherein R.sup.1 is C.sub.8 -C.sub.18 -alkyl or C.sub.8 -C.sub.18 -alkenyl, R.sup.2 is hydrogen or a group of the formula --CH.sub.2 COOM and M is alkaline or alkaline earth metal, which comprises heating a compound of the formula 2 ##STR2## at pH between 7-14, at a temperature of 80 to 90 deg C. and for at least 24 hours and subsequent reaction with an aqueous solution of chloroacetic acid or is alkali salt at a pH from 7 fo 14 and a temperature of 80 to 90.degree. C. Due to the long period for the ring opening in the first step predominantly secondary products are obtained which are advantageous in that they show a low viscosity of their aqueous solution.

REFERENCES:
Database CAPLUS on STN, Acc. No. 1992:407492, Sotodani et al., `Preparation fo amindoamine compounds with low discoloration.` JP 04026663 A2 (abstract), 1992.

Affiliated with

Also associated with

Rating

Process for making secondary amphoacetates and diacetates does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Process for making secondary amphoacetates and diacetates, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Process for making secondary amphoacetates and diacetates will most certainly appreciate the feedback.

Rate now

Comments { 0 }

Profile ID: LFUS-PAI-O-1907227