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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1675596Generated: October 26, 2026

4-(Ethylthio)benzaldehyde → [2-(Benzyloxy)-5-(trifluoromethyl)phenyl][4-(ethylthio)phenyl]methanol

https://huagongshe.com/reaction/1675596

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Ethylthio)benzaldehydeHCID 7006654—
Reactant1-(Benzyloxy)-2-bromo-4-(trifluoromethyl)benzeneHCID 18782669—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
Product[2-(Benzyloxy)-5-(trifluoromethyl)phenyl][4-(ethylthio)phenyl]methanolHCID 86659305—

Reaction Steps

A solution of butyl lithium (1.6M in hexane, 1.03 ml) was added to a stirred solution of the product from step (i) (0.5 g) in diethylether (20 ml) at −78° C. After 1 h, 4-ethylsulfanyl-benzaldehyde (0.25 g) was added and stirred for a further 1 h. The reaction was quenched with water, extracted with diethylether and the organic layer dried, then evaporated under reduced pressure. The residue was purified by chromatography on silica eluting with 50% diethylether/isohexane. Yield 0.7 g

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08003703B2
Source datasetuspto-grants-2011_08
ORD IDord-a467342c61aa494aa924692feb8515fc
Source noteuspto-grants-2011_08