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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638838Generated: October 31, 2026

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

https://huagongshe.com/reaction/638838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Imidazo[2,1-b][1,3]benzothiazol-2-yl)methanolHCID 2736621—
CatalystManganese dioxideHCID 14801—
SolventDichloromethaneHCID 6344—
ProductImidazo[2,1-b][1,3]benzothiazole-2-carbaldehydeHCID 4361913—

Reaction Steps

To a stirred solution of imidazo[2,1-b]-benzthiazole-2-methanol (2.04 g, 10 mmol) in methylene chloride (200 ml), activated MnO2 (15 g, excess) was added. The reaction mixture was stirred at room temperature for 24 h and filtered through a pad of celite. The reaction mixture was concentrated and the product was purified by silica gel column chromatography by eluting it with 75% ethyl acetate; hexane. Brown solid; Yield: 800 mg, 40%; M+H 203.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691842B2
Source datasetuspto-grants-2010_04
ORD IDord-321b54278d944c3d92deb974ab67bf9f
Source noteuspto-grants-2010_04