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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1252494Generated: November 3, 2026

Methanol → 1-(4'-Hydroxy-3'5'-difluorobenzyl)-2-(methylthio)imidazole

https://huagongshe.com/reaction/1252494

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBoron tribromideHCID 25134—
Reactant1-[(3,5-Difluoro-4-methoxyphenyl)methyl]-1,3-dihydro-2H-imidazole-2-thioneHCID 14450863—
SolventDichloromethaneHCID 6344—
Product1-(4'-Hydroxy-3'5'-difluorobenzyl)-2-(methylthio)imidazoleHCID 20140133—

Reaction Steps

A solution of 1-(4'-methoxy-3',5'-difluorobenzyl)-1,3-dihydro-2H-imidazole-2-thione (0.0046 mol) in 40 ml methylene chloride is treated with a solution of BBr3 (0.014 mol) in 10 ml methylene chloride. After four hours methanol is cautiously added, the mixture is stirred for an additional eighteen hours and the solvents are evaporated. The residue is dissolved in water, washed with ethyl acetate, neutralized with sodium bicarbonate, and extracted with ethyl acetate. The extracts are dried (MgSO4) and filtered and the solvent evaporated to yield 1-(4'-hydroxy-3'5'-difluorobenzyl)-2-(methylthio)imidazole. This compound then is substituted for 1-(4'-hydroxy-3',5'-difluorobenzyl)-1,3-dihydro-2H-imidazole-2-thione in the process of Example 1 to yield 1-(4'-acetoxy-3',5'-difluorobenzyl)-2-(methylthio)imidazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04743613
Source datasetuspto-grants-1988_05
ORD IDord-74bd5679caa44f69999dd1169ecc5115
Source noteuspto-grants-1988_05