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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1839298Generated: November 3, 2026

Benzoyl chloride → 7-Benzoylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1839298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantSodium CarbonateHCID 10340—
ReactantSodium SulfateHCID 24436—
ReactantAluminum(III) ChlorideHCID 6451240—
ReactantImidazo[5,1-b]thiazoleHCID 21262404—
SolventDichloromethaneHCID 6344—
SolventCarbon DisulfideHCID 6348—
Product7-Benzoylimidazo[5,1-b]thiazoleHCID 22632056—

Reaction Steps

Aluminum chloride (5.33 g) was added to a solution of 4.64 ml of benzoyl chloride in 50 ml of carbon disulfide. A solution of 1.24 g of imidazo[5,1-b]thiazole in 50 ml of dichloromethane was added dropwise thereto. The mixture was stirred at room temperature for 2 hr. The reaction solution was poured into 50 g of ice. Dichloromethane (100 ml) was added thereto. Sodium carbonate (16.7 g) and 16.7 g of sodium sulfate were added in that order to the mixture with stirring. The insolubles were removed by filtration through Celite, and then washed with dichloromethane. Filtrate was concentrated under the reduced pressure. The residue was purified by column chromatography on silica gel (hexane:ethyl acetate=5:1 to dichloromethane:ethyl acetate=2:1) to give 1.39 g of 7-benzoylimidazo[5,1-b]thiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06677331B2
Source datasetuspto-grants-2004_01
ORD IDord-5173fe91ebe141afba62b46513914ac4
Source noteuspto-grants-2004_01