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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1394695Generated: October 26, 2026

Benzyl Bromide → 1-(Benzyloxy)-3-ethylbenzene

https://huagongshe.com/reaction/1394695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant3-EthylphenolHCID 12101—
SolventDimethylformamideHCID 6228—
Product1-(Benzyloxy)-3-ethylbenzeneHCID 1974448593%

Reaction Conditions

Temperature2 °C

Reaction Steps

To a suspension of potassium carbonate (17 g, 123 mmol) in N,N-dimethylformamide (40 ml) was added a solution of 3-ethyl-phenol (14.8 ml, 123 mmol) in N,N-dimethylformamide (40 ml) at 2° C. under an argon atmosphere. After stirring for 50 min at 2° C., benzyl bromide (14.6 ml, 123 mmol) was added over a period of 15 min at 2° C. The suspension was stirred for additional 30 min at 2° C. and for 12 h at ambient temperature. After adding ice water (250 ml), the solution was extracted two times with diethyl ether. The combined extracts were washed two times with brine and dried over sodium sulfate. Evaporation of the solvent gave a yellow oil which was purified by column chromatography (silica gel, cyclohexane) to yield 24.3 g (114 mmol, 93%) of the title compound as yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07348349B2
Source datasetuspto-grants-2008_03
ORD IDord-02918c1dd0a5465495a99a800767ed7d
Source noteuspto-grants-2008_03