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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1745864Generated: October 31, 2026

Benzyl Bromide → 4-(Phenylmethoxy)benzenebutanol

https://huagongshe.com/reaction/1745864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantTetrahydrofuranHCID 8028—
ReactantTyrosolHCID 10393—
ReactantPotassium HydroxideHCID 14797—
CatalystTetrabutylammonium BromideHCID 74236—
Product4-(Phenylmethoxy)benzenebutanolHCID 15328765—

Reaction Steps

In a 250 ml reaction flask 2-(4-Hydroxyphenyl)-ethanol of formula, (5) (10 g, 0.07246 mol), potassium hydroxide (6.1 g, 0.1087 mol) and catalytic amount of phase transfer catalyst tetrabutyl ammonium bromide (0.150 g) was disssolved in 65 ml of THF. Stirred it for 1.5 hr. Benzyl bromide (8.6 ml, 0.07246 mol), was added to the reaction mixture dropwise. Stirred the reaction mixture at room temperature for 4 hrs. The progress of reaction was cheked by TLC. Filtered the reaction mixture and concentrated the filtrate on rota-vapour. The crude product was recrystalised from petroleum ether to afford 4-benzyloxy-(2-phenethyl ethanol) of formula (7), 14.9 g (90%) mp 85–86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07019172B2
Source datasetuspto-grants-2006_03
ORD IDord-0fce68d50c9c449dbc0e3b41cf8d9bf0
Source noteuspto-grants-2006_03