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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 888427Generated: October 25, 2026

Oxalyl chloride → 4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chloride

https://huagongshe.com/reaction/888427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant4,5,6,7-Tetrahydro-1-benzothiophene-2-carboxylic acidHCID 2063443—
CatalystDMF dimethylformamideHCID 17824068—
SolventDichloromethaneHCID 6344—
Product4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carbonyl chlorideHCID 6485362—

Reaction Conditions

Temperature0 °C

Reaction Steps

4,5,6,7-Tetrahydro-benzo[b]thiophene-2-carboxylic acid (1.0 g, 5.50 mmol) is dissolved in dichloromethane [DCM] (25 mL) that contains 5 drops of N,N-dimethylformamide dimethylformamide [DMF] under nitrogen and cooled to 0° C. Oxalyl chloride (13.7 mL of a 2.0M solution in ACM) is added via syringe and, allowed to warm to RT over 1 hour. All solvent is then removed under reduced pressure, and the resultant oil is reduced from toluene (3×20 mL) to remove residual oxalyl chloride. The residue is then dissolved in ethyl acetate and washed with saturated sodium bicarbonate (1×100 mL), then washed with saturated sodium chloride (1×100 mL) and dried over sodium sulfate. The solution is then filtered and concentrated under reduced pressure to give 4,5,6,7-tetrahydro-benzo[b]thiophene-2-carbonyl chloride (8) as an off-white solid (1.03 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247550B2
Source datasetuspto-grants-2012_08
ORD IDord-7e3449f1b0114adf835f25c7c6a279bf
Source noteuspto-grants-2012_08