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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1840435Generated: October 30, 2026

Benzyl Bromide → HCID 22631537, compound

https://huagongshe.com/reaction/1840435

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantAmmonium ChlorideHCID 25517—
Reactant7-Acetylthioimidazo[5,1-b]thiazoleHCID 22631663—
ReactantSodium methanolate methanolHCID 23694274—
SolventMethanolHCID 887—
ProductHCID 22631537HCID 22631537—

Reaction Steps

A solution of 396 mg of 7-acetylthioimidazo[5,1-b]thiazole in 2 ml of methanol was cooled in ice. A 1.018 M sodium methoxide/methanol solution (2.16 ml) was added to the cooled solution, and the mixture was stirred for 30 min. Benzyl bromide (0.262 ml) was added thereto, and the mixture was stirred at that temperature for 2 hr. An aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted with ethyl acetate twice. The organic layer was washed with brine twice, and was dried over anhydrous magnesium sulfate. The solvent was removed by distillation, and the residue was purified by column chromatography on silica gel (dichloromethane:methanol=30:1) to prepare 419 mg of 7-benzylthioimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06680313B2
Source datasetuspto-grants-2004_01
ORD IDord-b75e533d0ffa427395894507916ecc93
Source noteuspto-grants-2004_01