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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648035Generated: October 30, 2026

2-Chloroethyl Benzenesulfonate → 5-(2-Chloroethoxy)benzo[b]thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/648035

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl BenzenesulfonateHCID 13634485—
ReactantMethyl 5-hydroxybenzo[b]thiophene-2-carboxylateHCID 13662999—
SolventMethanolHCID 887—
SolventSodiumHCID 5360545—
Product5-(2-Chloroethoxy)benzo[b]thiophene-2-carboxylic acid methyl esterHCID 1366300038.7%

Reaction Steps

5-Hydroxybenzo[b]thiophene-2-carboxylic acid methyl ester (1.47 g.) was dissolved in a solution of sodium (0.163 g.) in methanol (15 ml.) and 2-(benzenesulphonyloxy)ethyl chloride (1.57 g.) was added. The resulting solution was heated under reflux for 8 hours and then allowed to cool and stood overnight. The solution was then evaporated and the residue was partitioned between water and ether. The aqueous layer was separated and washed several times with ether. The combined organic layer and ethereal extracts were washed with water, dried (Na2SO4) and evaporated. The residue was chromatographed on silica gel. Elution with chloroform gave a solid which was crystallized from ethyl acetate/petrol (b.p. 60°-80°) to give 5-(2-chloroethoxy)benzo[b]-thiophene-2-carboxylic acid methyl ester, (0.74 g.), m.p. 116°-117° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04410539
Source datasetuspto-grants-1983_10
ORD IDord-263a9902110f4542aeb3a05a1f436f00
Source noteuspto-grants-1983_10