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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1740593Generated: October 29, 2026

Carbon tetrabromide → 2-(Trifluoromethoxy)benzyl bromide

https://huagongshe.com/reaction/1740593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantTriphenylphosphineHCID 11776—
Reactant2-(Trifluoromethoxy)benzyl alcoholHCID 2777245—
SolventDiethyl EtherHCID 3283—
Product2-(Trifluoromethoxy)benzyl bromideHCID 2777254—

Reaction Steps

To a stirred solution of 2-trifluoromethoxybenzyl alcohol (0.81 g, 4.5 mmol) from Step 1 above in ether (20 mL) at 0° C. was added triphenylphosphine (2.4 g, 9.2 mmol) and CBr4 (3.0 g, 9.2 mmol). The mixture was warmed to ambient temperature and stirred for 18 h. The ether was decanted from the gummy precipitate of triphenylphosphine oxide and evaporated under reduced pressure. The residue was purified by pressurized silica gel column chromatography using hexanes as eluant to give 2-trifluoromethoxybenzyl bromide as a colorless liquid (TLC Rf =0.80 (hexanes)).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05968938
Source datasetuspto-grants-1999_10
ORD IDord-9121b104c65a455fa81be3fc4bb025dd
Source noteuspto-grants-1999_10