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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183595Generated: October 30, 2026

Sodium borohydride → HCID 9857138, compound

https://huagongshe.com/reaction/2183595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 22473925HCID 22473925—
SolventMethanolHCID 887—
ProductHCID 9857138HCID 985713886.9%

Reaction Steps

Sodium borohydride (0.05 g) was added in portions over 2 minutes to a stirred suspension of 3-(benzo[b]thiophen-4-yl)-5,6-dihydroimidazo[2,1-b]thiazole-2-carboxaldehyde (0.36 g) in methanol (10 ml), then the mixture was stirred at ambient temperature for 1.5 hours. The solvent was removed in vacuo then water (20 ml) and ethyl acetate (30 ml) were added and the mixture was stirred at ambient temperature for 2 hours. The aqueous phase was separated and washed with ethyl acetate (30 ml), then the combined ethyl acetate solutions were dried (MgSO4) and the solvent was removed in vacuo at 60° C. to give [3-(benzo[b]thiophen-4-yl)-5,6-dihydroimidazo[2,1-b]thiazol-2-yl]methanol (0.315 g) as a cream solid, m.p. 145-149° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06900216B2
Source datasetuspto-grants-2005_05
ORD IDord-958abc5ee033498e93a9b4f02c99796c
Source noteuspto-grants-2005_05