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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356721Generated: October 29, 2026

Oxalyl chloride → 5-Carboethoxythiophen-2-carbonyl chloride

https://huagongshe.com/reaction/356721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant5-(Ethoxycarbonyl)thiophene-2-carboxylic acidHCID 15232123—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-Carboethoxythiophen-2-carbonyl chlorideHCID 10262858—

Reaction Steps

To a suspension of acid 35 (0.64 g, 3.2 mmol) in dichloromethane (20 mL) under argon at room temperature was added a 2.0M solution of (COCl)2 in dichloromethane (2.4 mL, 4.8 mmol) and two drops of DMF, and stirred overnight. Excess (COCl)2 and dichloromethane were removed at reduced pressure, and the viscous, light, yellow product was dried overnight to afford the desired benzoyl chloride 36 as a yellow solid. The structure of the product was also confirmed using IR and 1H NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05837725
Source datasetuspto-grants-1998_11
ORD IDord-e97b5a575fb346c99bba8ebb8b03ff6e
Source noteuspto-grants-1998_11