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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572820Generated: October 31, 2026

Benzaldehyde → Diisopropyl Ether

https://huagongshe.com/reaction/572820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantBenzothiazoleHCID 7222—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductDiisopropyl EtherHCID 7914—
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 balloon 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 oxide affords benzothiazol-2-ylphenylmethanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09029357B2
Source datasetuspto-grants-2015_05
ORD IDord-a26dd57dca6a4cd4be961b63d2cc5f84
Source noteuspto-grants-2015_05