Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116678Generated: October 27, 2026

Acetic Anhydride → (E)-2-acetylamino-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acrylic acid

https://huagongshe.com/reaction/2116678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantAcetylglycineHCID 10972—
ReactantSodium AcetateHCID 517045—
Reactant4-Amino-3-chloro-5-(trifluoromethyl)benzaldehydeHCID 13020473—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product(E)-2-acetylamino-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acrylic acidHCID 66941463—

Reaction Conditions

Temperature128 °C

Reaction Steps

A mixture of 50.0 g (224 mmol) 4-amino-3-chloro-5-trifluoromethyl-benzaldehyde, 39.3 g (335 mmol) N-acetylglycine, 27.5 g (335 mmol) sodium acetate and 200 ml acetic anhydride was stirred for 2 hours in an oil bath at an oil bath temperature of 128° C. After cooling to an oil bath temperature of 90° C. 100 ml of water were added dropwise and the resulting suspension was added to a mixture of 1000 ml of water and 500 ml of toluene. The precipitate formed was suction filtered, washed with 300 ml of toluene and 500 ml of water and dried overnight at 60° C. in the circulating air dryer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439237B2
Source datasetuspto-grants-2008_10
ORD IDord-10dfa442898848b5a73b028f43127b1b
Source noteuspto-grants-2008_10