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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1585448Generated: November 2, 2026

Hydrochloric Acid → 2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehyde

https://huagongshe.com/reaction/1585448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTolueneHCID 1140—
ReactantEthyl 2,3-dihydroimidazo[2,1-b]thiazole-6-carboxylateHCID 18183084—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2,3-Dihydroimidazo[2,1-b][1,3]thiazole-6-carbaldehydeHCID 1124060443%

Reaction Conditions

Temperature-70 °C

Reaction Steps

Ethyl 2,3-dihydroimidazo[2,1-b]thiazole-6-carboxylate (4.2 g; 21.21 mmol) was dissolved in dry dichloromethane (150 ml) and cooled to -70° C. under a stream of dry argon. This solution was treated with a solution of diisobutylaluminium hydride in toluene (1.5M, 26.9 ml, 2 equivalents) over 40 minutes at -70° C. The reaction mixture was stirred at -70° C. for a further 0.5 h. Water (10 ml) was added and the mixture stirred at ambient temperature for 0.5 hr. The mixture was acidified with 5M HCl, filtered through a celite pad and the pad further washed with dichloromethane. The combined organic extracts were dried over anhydrous magnesium sulphate and evaporated to dryness. Chromatography on silica gel, eluting with ethyl acetate, gave the title compound (1.4 g, 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05939066
Source datasetuspto-grants-1999_08
ORD IDord-304efc5a9a0d4812881dacea9d4064b3
Source noteuspto-grants-1999_08