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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106655Generated: October 31, 2026

Benzyl Bromide → 4-Benzyloxyphenylacetonitrile

https://huagongshe.com/reaction/1106655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Hydroxybenzyl cyanideHCID 26548—
SolventAcetoneHCID 180—
SolventEthyl AcetateHCID 8857—
Product4-BenzyloxyphenylacetonitrileHCID 52280495.4%

Reaction Steps

4-Hydroxybenzyl cyanide (2.5 g, 18.77 mmol), benzyl bromide (3.8 g, 22.5 mmol) and potassium carbonate (45 mmol) were combined in acetone (50 mL) and heated to reflux for 8 h. The reaction was allowed to cool to rt, diluted with ethyl acetate and filtered to remove the solids. The organic layer was concentrated in vacuo to give an oil. The crude benzyl ether was purified by chromatography on silica gel eluting hexane: ethyl acetate (90:10, v:v) to give 4-benzyloxybenzyl cyanide (4.0 g, 95%) which solidified. MS (M+NH4)+ =241.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057336
Source datasetuspto-grants-2000_05
ORD IDord-79719caa7a1446dbacaf5502c04cc61f
Source noteuspto-grants-2000_05