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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2277421Generated: October 30, 2026

Cyanoacetic acid → HCID 70873402, compound

https://huagongshe.com/reaction/2277421

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyanoacetic acidHCID 9740—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 43217378HCID 43217378—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventSodium bicarbonate waterHCID 86585896—
ProductHCID 70873402HCID 70873402—

Reaction Steps

To a stirred mixture of commercially available cyanoacetic acid (1 eq, 0.170 g, 2.0 mmole) in dichloromethane was added oxalylchloride (0.253 g, 2.0 mmole, 0.169 mL) and 2 drops dimethylformamide. The reaction was stirred for 2 hours at RT until homogenous solution developed. 2-(4-Fluoro-benzylamino)-benzoic acid ethyl ester (1 eq, 0.500 g, 1.82 mmole) was added and the resulting solution, was allowed to stir at RT overnight. Reaction mixture was diluted with saturated sodium bicarbonate water (20 mL) and extracted with ethyl acetate (25 mL×3). Combined organic phase was washed consecutively with water, brine before drying over sodium sulfate. Organic phase was evaporated and the residue was purified by flash chromatography to afford 2-[(2-Cyano-acetyl)-(4-fluoro-benzyl)-amino]-benzoic acid ethyl ester as an off white solid (0.423 g, 68%, LCMS calc M+H 341, obs M+H 341).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133164B2
Source datasetuspto-grants-2015_09
ORD IDord-f5e13ead66f7428a8f3fe50376dc2efe
Source noteuspto-grants-2015_09