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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093318Generated: November 1, 2026

Triphenylphosphine → 3-Benzyloxybenzyl bromide

https://huagongshe.com/reaction/1093318

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
Reactant3-(Phenylmethoxy)benzenemethanolHCID 74341—
SolventDichloromethaneHCID 6344—
Product3-Benzyloxybenzyl bromideHCID 150204788.9%

Reaction Steps

3-Benzyloxybenzyl alcohol (5.00 g) was dissolved in methylene chloride (70 ml), triphenylphosphine (6.52 g) and N-bromosuccinimide (4.43 g) were added under ice-cooling, and the mixture was stirred under ice-cooling for 1 hr, and further at room temperature for 4 hr. The reaction mixture was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. Diethyl ether (100 ml) was added, and the precipitated triphenylphosphine oxide was filtered off. The concentrate of the filtrate was purified by silica gel column chromatography (hexane:ethyl acetate=10:1) to give the object product (5.75 g) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129361B2
Source datasetuspto-grants-2012_03
ORD IDord-9568c2bdb2c54fa48f3b966635a9fea8
Source noteuspto-grants-2012_03