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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2375133Generated: October 31, 2026

Benzyl Bromide → 4-(3-Benzyloxypropyl)bromobenzene

https://huagongshe.com/reaction/2375133

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantAmmonium ChlorideHCID 25517—
Reactant3-(4-Bromophenyl)propan-1-olHCID 10560614—
SolventBenzeneHCID 241—
Product4-(3-Benzyloxypropyl)bromobenzeneHCID 21909326—

Reaction Steps

A suspension of sodium hydride (60%, 0.97 g), 3-(4-bromophenyl)-1-propanol (1.0 g) and benzyl bromide (0.69 mL) in benzene (24 mL) was stirred for 7 hours under reflux. After cooling to ambient temperature, a saturated aqueous ammonium chloride solution (50 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (100 mL). The organic layer was washed with water (40 mL) and brine (40 mL), and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: hexane/ethyl acetate=20/1) to give 4-(3-benzyloxypropyl)bromobenzene (1.4 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07465712B2
Source datasetuspto-grants-2008_12
ORD IDord-b7ac4fd27b1e45c5a1e80a0f280b7e80
Source noteuspto-grants-2008_12