Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337156Generated: October 30, 2026

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

https://huagongshe.com/reaction/337156

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 numberUS08889692B2
Source datasetuspto-grants-2014_11
ORD IDord-9f3d0f08c1194ad59fd5df6303fab2e7
Source noteuspto-grants-2014_11