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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383503Generated: October 30, 2026

Bromocyclopentane → Methyl 3-cyclopentyloxy-4-(methylthio)benzoate

https://huagongshe.com/reaction/1383503

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromocyclopentaneHCID 8728—
ReactantSodium hydrideHCID 24758—
ReactantMethyl 3-hydroxy-4-(methylthio)benzoateHCID 21187893—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-cyclopentyloxy-4-(methylthio)benzoateHCID 2118794471.4%

Reaction Steps

A stirred solution of methyl 3-hydroxy-4(methylthio)benzoate (1.98 g) in dry dimethylformamide (40 mL) is treated with sodium hydride (0.44 g; 60% dispersion in mineral oil; 11 mmol) and the solution is stirred for a further 25 minutes. The reaction mixture is treated with cyclopentyl bromide (1.64 g), stirred at 60° C. for 3 hours. and then concentrated. The resulting residue is partitioned between dichloromethane (50 mL) and water (50 mL), the aqueous layer is extracted with dichloromethane (50 mL), and the combined organic layers are dried and concentrated, to give a red oil. The oil is subjected to flash chromatography, eluting with a mixture of diethyl ether and pentane (1:9 v/v), to give methyl 3-cyclopentyloxy-4-(methylthio)benzoate (1.9 g), m.p. 53-55° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255326B1
Source datasetuspto-grants-2001_07
ORD IDord-07e91960a00a4e9cb461921dd423158f
Source noteuspto-grants-2001_07