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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1263611Generated: November 3, 2026

Oxalyl chloride → 5-(3,4-Dichlorobenzyl-carbamoyl)-thiophene-2-carbonyl-chloride

https://huagongshe.com/reaction/1263611

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-(3,4-Dichlorobenzyl-carbamoyl)-thiophene-2-carboxylic acidHCID 18617115—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(3,4-Dichlorobenzyl-carbamoyl)-thiophene-2-carbonyl-chlorideHCID 18617125—

Reaction Steps

A stirring solution of (12(b)) (495 mg; 1.5 mmole) in dichloromethane (25 mL) was cooled in an ice bath and DMF (1 drop) and oxalyl chloride (0.175 mL: 2.0 mmole) added dropwise. The solution was stirred at ambient temperature under argon for 4 hours. The dichloromethane and excess oxalyl chloride were removed in vacuo. The residue was azeotroped with toluene (2×15 mL) to give 5-(3,4-dichlorobenzyl-carbamoyl)-thiophene-2-carbonyl-chloride (12(c)) which was used crude in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541491B1
Source datasetuspto-grants-2003_04
ORD IDord-3d06ff1860754c5ba3c07c32d873f40a
Source noteuspto-grants-2003_04