Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082772Generated: October 26, 2026

Benzoyl chloride → N-(3-Carboxymethyl-5-phenyl-2-thienyl)-benzamide

https://huagongshe.com/reaction/2082772

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantMethyl cyanoacetateHCID 7747—
ReactantMethyl 2-amino-5-phenylthiophene-3-carboxylateHCID 705256—
ReactantN-(3-Carboxymethyl-5-phenyl-2-thienyl) cyclohexane carboxamideHCID 23341632—
SolventWaterHCID 962—
SolventHexamethylphosphoramideHCID 12679—
ProductN-(3-Carboxymethyl-5-phenyl-2-thienyl)-benzamideHCID 23341625—

Reaction Steps

Methyl 2-amino-5-phenyl-thiophene-3-carboxylate (1.3 g, 0.0055 mole) in hexamethyl phosphoramide (prepared by the method of Chemische Berichte, 99, 94 (1966) but using methyl cyanoacetate in place of ethyl cyanoacetate) (20 ml.) was stirred and treated with benzoyl chloride (1.56 g, 1.28 ml, 0.011 mole). The solution was stirred for 2 hours, poured into water (750 ml), stored overnight and the title compound filtered off (1.31 g) m.p. 190° C. Similarly prepared was: N-(3-Carboxymethyl-5-phenyl-2-thienyl) cyclohexane carboxamide, m.p. 121°-122° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04082771
Source datasetuspto-grants-1978_04
ORD IDord-47bb0a7efc064b86a30d65c93c0fa913
Source noteuspto-grants-1978_04