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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720955Generated: November 1, 2026

Water → Ethyl 5-chloro-3-methyl-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/1720955

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl chloroformateHCID 10928—
Reactant19404-18-3HCID 317317—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventHexaneHCID 8058—
ProductEthyl 5-chloro-3-methyl-1-benzothiophene-2-carboxylateHCID 1483626067%

Reaction Conditions

Temperature0 °C

Reaction Steps

n-Butyllithium in hexane (2.6M, 2.3 ml) was added to a solution of 5-chloro-3-methylbenzo(b)thiophene (1.0 g, 6 mmol) in ethyl ether (20 ml) stirred at 0° C. under argon. The mixture was stirred for 30 minutes and transferred slowly under argon pressure to a stirred solution of ethyl chloroformate (0.63 g, 6 mmol) in ethyl ether (20 ml). The mixture was stirred at 0° C. for 30 minutes and at 25° C. for 1.5 hours. The mixture was treated with water and the organic phase was dried, concentrated and triturated with hexane to give 1.0 g (67%) of ethyl 5-chloro-3-methylbenzo(b)thiophene-2-carboxylate: mp 92.5°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05508306
Source datasetuspto-grants-1996_04
ORD IDord-2ef19a15965149f8a058572a6339f22b
Source noteuspto-grants-1996_04