Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1858165Generated: October 25, 2026

2-Thiopheneacetyl chloride → Methyl 4-chloro-5-nitro-2-(2-(thiophen-2-yl)acetamido)benzoate

https://huagongshe.com/reaction/1858165

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiopheneacetyl chlorideHCID 162362—
ReactantMethyl 2-amino-4-chloro-5-nitrobenzoateHCID 15895692—
ProductMethyl 4-chloro-5-nitro-2-(2-(thiophen-2-yl)acetamido)benzoateHCID 5405596767.6%

Reaction Steps

To a suspension of 2-amino-4-chloro-5-nitrobenzoic acid methyl ester (221 mg in 2.5 mL of dry 1,2-dichloroethane) was added a solution of thiophen-2-yl-acetyl chloride (169 mg in 3.0 mL dry 1,2-dichloroethane) and the mixture heated at reflux on an oil bath. After 18 hours, the reaction was cooled and the solvent removed in vacuo. Recrystallization of the crude product from methanol gave the title compound (230 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06150522
Source datasetuspto-grants-2000_11
ORD IDord-3360fadb200f44918fa5a528d8f1207f
Source noteuspto-grants-2000_11