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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 258163Generated: October 30, 2026

Tetrahydrofuran → [2-(2,5-Difluorobenzylthio)phenyl]acetic acid

https://huagongshe.com/reaction/258163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2-(Bromomethyl)-1,4-difluorobenzeneHCID 522830—
ReactantBenzo[b]thiophen-2(3H)-oneHCID 591560—
Product[2-(2,5-Difluorobenzylthio)phenyl]acetic acidHCID 19782617—

Reaction Steps

A mixture of benzo[b]thiophen-2(3H)-one (11.2 g) aqueous sodium hydroxide (5.58 g in 100 ml water) and tetrahydrofuran (10 ml) was heated under reflux for two hours. A solution of 2,5-difluorobenzyl bromide (15.5 g) in tetrahydrofuran (10 ml) was added and the mixture refluxed for a further 2 hours and allowed to cool. The aqueous layer was clarified by ether extraction and then acidified with concentrated hydrochloric acid. The precipitate was collected, washed with water and dried. The solid was recrystallised from dipropyl ether/hexane to give [2-(2,5-difluorobenzylthio)phenyl]acetic acid, mp 106.5°-107.5°. A solution of this product (14.4 g) in methanol (150 ml) containing concentrated sulphuric acid (0.5 ml) was heated under reflux for 4 hours, cooled and evaporated. The residue was dissolved in ethyl acetate/ether and washed with water and aqueous sodium bicarbonate, dried and evaporated to give methyl [2-(2,5-difluorobenzylthio)phenyl]acetate, as a light brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05264609
Source datasetuspto-grants-1993_11
ORD IDord-a43cf7bd732046d19876d5b00aa6b74d
Source noteuspto-grants-1993_11