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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474677Generated: November 1, 2026

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

https://huagongshe.com/reaction/1474677

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 numberUS09018224B2
Source datasetuspto-grants-2015_04
ORD IDord-307e7b63164c4ab18b8c90b4bdcb4376
Source noteuspto-grants-2015_04