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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1534627Generated: November 4, 2026

Thiophenol → HCID 67900867, compound

https://huagongshe.com/reaction/1534627

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThiophenolHCID 7969—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 14565731HCID 14565731—
CatalystTetrabutylammonium BromideHCID 74236—
SolventWaterHCID 962—
ProductHCID 67900867HCID 67900867—

Reaction Steps

A mixture of thiophenol (0.7 g, 6.36 millimole), ethyl 2-chloro-3-methyl-3-butenoate (1.05 g, 6.5 millimole), tetrahydrofuran (2 ml), and tetrabutyl ammonium bromide (50 mg) was stirred at room temperature while one equivalent (1.5 ml) of 4N NaOH was added rapidly. Stirring of the resulting two-phase system was continued for two hours (at room temperature). The reaction mixture was diluted with 50 ml of water and extracted twice with 20 ml proportions of ether. Evaporation of the ether left 1.4 g of a crude yellow oil. Flash column chromatography on silica gel gave the desired product, ethyl 2-thiophenyl-3-methyl-2-butenoate in 66% overall yield. The identity of the product was confirmed by proton NMR, carbon 13 NMR, and mass spectrum analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05089611
Source datasetuspto-grants-1992_02
ORD IDord-63058a0d81b449219ee2883f1510581f
Source noteuspto-grants-1992_02