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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084367Generated: October 29, 2026

Benzyl Bromide → 4-(Phenylmethoxy)benzenebutanol

https://huagongshe.com/reaction/2084367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantPotassium bisulfateHCID 516920—
Reactant4-(4-Hydroxybutyl)phenolHCID 13392513—
SolventDimethylformamideHCID 6228—
Product4-(Phenylmethoxy)benzenebutanolHCID 1532876573.4%

Reaction Steps

In an argon atmosphere, dry DMF (115 ml) was added to 4-(4-hydroxybutyl)phenol (9.43 g) and 65% oily sodium hydride (2.4 g), followed by stirring for 15 minutes. Next, under ice cooling and stirring, a solution of benzyl bromide (9.87 g) in dry dimethylformamide (29.5 ml) was added drop by drop, followed by stirring at the same temperature for 2 hours. After ice water and a 1 N solution of potassium hydrogen sulfate were added, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated saline, after which it was dried with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure; the residue was purified by silica gel column chromatography to yield the titled compound (10.67 g) as a colorless crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716863B2
Source datasetuspto-grants-2004_04
ORD IDord-9f31a58e6a98460ead37c6d8817eddf6
Source noteuspto-grants-2004_04