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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638837Generated: October 30, 2026

ethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylate → (Imidazo[2,1-b][1,3]benzothiazol-2-yl)methanol

https://huagongshe.com/reaction/638837

Reaction equation

Participants

RoleNameHCIDCharge
Reactantethyl imidazo[2,1-b][1,3]benzothiazole-2-carboxylateHCID 1480574—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product(Imidazo[2,1-b][1,3]benzothiazol-2-yl)methanolHCID 2736621—

Reaction Steps

To a stirred slurry of LiAlH4 (2.0 g, excess) in dry THF, ethyl imidazo[2,1-b]-benzthiazole-2-carboxylate (4.9 g, 20 mmol) was slowly added in THF (100 ml) at 0° C. After the addition, the reaction mixture was stirred at room temperature for 1 h and quenched with saturated NH4Cl/NH4OH. The separated solid was diluted with Chloroform/MeOH (3:1) and filtered through a pad of celite. The organic layer was washed once with saturated NaCl and dried over anhydrous MgSO4. It was filtered and concentrated. The brown solid obtained was taken to next step with out purification. Yield: 3.8 g, 93%; M+H 205; mp 131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691842B2
Source datasetuspto-grants-2010_04
ORD IDord-ff51e18a5b32430c83d6930fa1121870
Source noteuspto-grants-2010_04