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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1744917Generated: November 2, 2026

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

https://huagongshe.com/reaction/1744917

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]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 numberUS07018997B2
Source datasetuspto-grants-2006_03
ORD IDord-85db9eb1b35e4f54a1414215be7c3ece
Source noteuspto-grants-2006_03