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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 330257Generated: October 31, 2026

Sodium Cyanide → (5-Bromo-2-naphthalenyl)acetonitrile

https://huagongshe.com/reaction/330257

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CyanideHCID 8929—
Reactant1-Bromo-6-(bromomethyl)naphthaleneHCID 11324032—
SolventAcetonitrile--water (1/1)HCID 18373917—
Product(5-Bromo-2-naphthalenyl)acetonitrileHCID 1986967399.1%

Reaction Steps

A suspension of 5-bromo-2-bromomethylnaphthalene (4.50 g, 15 mmol) and NaCN (784 mg, 16 mmol) in 9:1 CH3CN/H2O (150 mL) was heated to reflux for 1 hour during which time the reaction mixture became homogeneous. The solution was cooled to room temperature and the volatiles removed in vacuo. The aqueous residue was partitioned between H2O (200 mL) and CH2Cl2 (200 mL). The aqueous phase was further washed with CH2Cl2 (1×200 mL) and the combined organic layers dried (Na2SO4) and concentrated in vacuo to give the product as a white solid (3.66 g, 99%). This material was of sufficient purity to be used as such without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04895861
Source datasetuspto-grants-1990_01
ORD IDord-c31b33663eb7486197f1f27d5a9411b6
Source noteuspto-grants-1990_01