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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444184Generated: October 26, 2026

Toluene → 2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazole

https://huagongshe.com/reaction/1444184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantPotassium sodium tartarateHCID 9855836—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantEthyl 2-bromoimidazo[5,1-b]thiazole-7-carboxylateHCID 59168405—
SolventDichloromethaneHCID 6344—
Product2-Bromo-7-hydroxymethylimidazo[5,1-b]thiazoleHCID 5916840699%

Reaction Steps

A solution of ethyl 2-bromoimidazo[5,1-b] thiazole-7-carboxylate (101 mg, 0.37 mmol) in dichloromethane (5 ml) was cooled to −50° C. A toluene solution of diisobutylaluminium hydride (1.01 M solution; 1.1 ml, 1.1 mmol) was then added dropwise to the cooled solution, and the mixture was stirred at the same temperature for 10 min. After the completion of the reaction, a saturated aqueous potassium sodium tartrate solution was added thereto, and the mixture was stirred at room temperature for one hr and was extracted with ethyl acetate (7 ml×3). The organic layer was washed with saturated brine and was dried over anhydrous sodium sulfate, and the solvent was removed by distillation under the reduced pressure to give 2-bromo-7-hydroxymethylimidazo[5,1-b]thiazole (85 mg, 99%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662841B2
Source datasetuspto-grants-2010_02
ORD IDord-b9e31d92e2654e489578c86435f03f29
Source noteuspto-grants-2010_02