Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 844158Generated: October 30, 2026

Dimethylformamide → 3-Chloro-5-methylthiophene-2-carbonyl chloride

https://huagongshe.com/reaction/844158

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Chloro-5-methylthiophene-2-carboxylic acidHCID 16640001—
SolventDichloromethaneHCID 6344—
Product3-Chloro-5-methylthiophene-2-carbonyl chlorideHCID 18376862101%

Reaction Steps

To a suspension of 2-carboxy-3-chloro-5-methylthiophene (1.2 g, 6.6 mmol) in methylene chloride (16 mL) at 0° C. were added oxalyl chloride (0.6 mL, 7.3 mmol) and a drop of DMF. The mixture was stirred at ambient temperature for 5 hours, then concentrated of all volatiles and dried in vacuo to afford 1.3 g (quantitative yield) of 2-chlorocarbonyl-3-chloro-5-methylthiophene as a pale yellow solid; NMR (DMSO-d6/TFA) 7.4 (s, 1), 2.5 (s, 3) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06380221B1
Source datasetuspto-grants-2002_04
ORD IDord-3db0c2fe1c4e4c54bc99775bd1bc0d11
Source noteuspto-grants-2002_04