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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370089Generated: October 30, 2026

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

https://huagongshe.com/reaction/370089

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 numberUS06140351
Source datasetuspto-grants-2000_10
ORD IDord-1e1863ebb6b748a9965212deca45180b
Source noteuspto-grants-2000_10