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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850725Generated: November 4, 2026

Benzyl Bromide → 5-(Benzyloxy)-2-bromobenzonitrile

https://huagongshe.com/reaction/1850725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Bromo-5-hydroxybenzonitrileHCID 15323111—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-(Benzyloxy)-2-bromobenzonitrileHCID 12101986—

Reaction Steps

4-bromo-3-cyanophenol (1 g, 5.05 mmol) was dissolved in DMF (10 ml) and K2CO3 (1.40 g, 10.10 mmol) and benzyl bromide (0.66 ml, 5.56 mmol) added. The mixture was stirred under N2 for 1 hr at RT. The mixture was diluted with water (15 mL) and extracted with EtOAc (2×10 mL). The organic fractions were combined, washed with brine (saturated, 1×8 mL), dried over MgSO4, filtered and the volatiles removed in vacuo. The residue was purified by chromatography on silica gel Biotage 25M, using a gradient eluant of EtOAc/Hexane (0-50%) to afford the title compound. LC/MS (m/z): 289 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957062B2
Source datasetuspto-grants-2015_02
ORD IDord-f4ebb45edb8e4e43989e82cd627d0888
Source noteuspto-grants-2015_02