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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404408Generated: November 1, 2026

Benzaldehyde → Benzothiazol-2-yl-phenyl-methanol

https://huagongshe.com/reaction/2404408

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzothiazoleHCID 7222—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductBenzothiazol-2-yl-phenyl-methanolHCID 257798—

Reaction Conditions

Temperature-20 °C

Reaction Steps

A solution of benzothiazole (1.35 g) in tetrahydrofurane (10 mL) in a dried round bottom baloon is cooled at −70° C. A solution of butyl lithium (4.1 mL) is added and the mixture stirred for 15 minutes. Benzaldehyde (1.03 mL) diluted with tetrahydrofurane (10 mL) is then added. The mixture is stirred at −70° C. for 1 h, allowed to warm to −20° C. and quenched with saturated aqueous ammonium chloride solution. The mixture is extracted with ethyl acetate. Organic extracts are pooled, dried over magnesium sulfate and concentrated under reduced pressure. Trituration of the residue with diisopropyl oxyde affords benzothiazol-2-ylphenylmethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802664B2
Source datasetuspto-grants-2014_08
ORD IDord-19108a02a6d44e2ca850634076d4fedc
Source noteuspto-grants-2014_08