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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 890954Generated: October 30, 2026

Water → 7-(Benzyloxy)naphthalene-2-carbonitrile

https://huagongshe.com/reaction/890954

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant7-Hydroxynaphthalene-2-carbonitrileHCID 22243621—
SolventDimethyl SulfoxideHCID 679—
Product7-(Benzyloxy)naphthalene-2-carbonitrileHCID 2224342890.3%

Reaction Steps

Sodium hydride (151 mg, 60% in mineral oil, 3.77 mmol) is added to a stirring solution of 7-hydroxy-2-naphthonitrile (530 mg, 3.14 mmol) in DMSO (10 mL). After the bubbling subsides, benzyl bromide (448 μL, 3.77 mmol) is added and the resulting mixture is allowed to stir for 4 hours. The reaction mixture is poured into water and extracted with ether. The ether layer is dried (Na2SO4), filtered, and concentrated to dryness. The product is purified by column chromatography (step gradient, 25 to 50% CH2Cl2 in hexanes) to give 7-benzyloxy-2-naphthonitrile (735 mg, 90%) as a white solid. HRMS (EI) calculated for C18H13NO: 259.0997, found 259.0993.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07001900B2
Source datasetuspto-grants-2006_02
ORD IDord-312464c0cc5c458b901921ecf26e109d
Source noteuspto-grants-2006_02