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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638954Generated: November 2, 2026

Benzyl Bromide → 1-(Benzyloxy)-4-bromo-2-[(trifluoromethyl)sulfanyl]benzene

https://huagongshe.com/reaction/638954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
Reactant4-Bromo-2-[(trifluoromethyl)sulfanyl]phenolHCID 68685673—
Product1-(Benzyloxy)-4-bromo-2-[(trifluoromethyl)sulfanyl]benzeneHCID 68686861—

Reaction Steps

1-Benzyloxy-4-bromo-2-trifluoromethylthiobenzene was prepared from 4-bromo-1-hydroxy-2-trifluoromethylthiobenzene following Method C. The reaction was conducted at 50° C. for 1 h using benzyl bromide as an alkylating agent and the resulting product was purified by column chromatography using hexanes as an eluent to afford 1-benzyloxy-4-bromo-2-trifluoromethylthiobenzene in 63% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07691843B2
Source datasetuspto-grants-2010_04
ORD IDord-9062141baf054398915a59a2aed7b2d4
Source noteuspto-grants-2010_04