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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697414Generated: November 2, 2026

Benzyl Bromide → 2-(3-(Benzyloxy)propyl)benzonitrile

https://huagongshe.com/reaction/1697414

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Hydroxypropyl)benzonitrileHCID 66689952—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product2-(3-(Benzyloxy)propyl)benzonitrileHCID 66688699—

Reaction Steps

A solution of 2-(3-hydroxypropyl)benzonitrile (Example 323c, 3.83 g) in DMF (40 mL) under nitrogen was treated with 60% Sodium hydride (1.140 g) and stirred at room temperature for 1 h before adding benzyl bromide (2.83 mL). The resulting solution was stirred at 20° C. for 60 h. The reaction mixture was diluted with water (200 mL), and extracted with ethyl acetate (200 mL). The organic was dried (MgSO4), filtered and evaporated. The residue was purified (SiO2 chromatography eluting with 30% diethyl ether in isohexane). Pure fractions were evaporated to dryness to afford the subtitle compound as an oil (2.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163905B2
Source datasetuspto-grants-2012_04
ORD IDord-3f82f10ccc2b485b996f6aabc890fe96
Source noteuspto-grants-2012_04