Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1977358Generated: October 31, 2026

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

https://huagongshe.com/reaction/1977358

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 uith 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 numberUS06232338B1
Source datasetuspto-grants-2001_05
ORD IDord-c40991672c294059942cac1dbff3f3dd
Source noteuspto-grants-2001_05