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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2169377Generated: November 2, 2026

Ethyl Acetate → (1-Naphthalen-1-yl-cyclopentyl)-acetonitrile

https://huagongshe.com/reaction/2169377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CyanideHCID 8929—
ReactantMethanesulfonic acid 1-naphthalen-1-yl-cyclopentylmethyl esterHCID 86726006—
SolventDimethyl SulfoxideHCID 679—
SolventHexaneHCID 8058—
Product(1-Naphthalen-1-yl-cyclopentyl)-acetonitrileHCID 8672600744%

Reaction Steps

To a stirred solution of methanesulfonic acid 1-naphthalen-1-yl-cyclopentylmethyl ester (341) (2.1 g, 6.90 mmol) in dimethyl sulfoxide (10.0 mL) were added KI (115 mg, 0.69 mmol) and NaCN (507 mg, 10.35 mmol) and the reaction mixture was stirred at 140° C. for 2 h (silica TLC, 10% ethyl acetate in hexane; Rf=0.5). The reaction mass was cooled to room temperature, quenched with FeSO4 solution (15 mL) and diluted with water (100 mL). The resulting solid was separated through filtration and washed well with ethyl acetate. The biphasic layer was separated in a separating funnel. The organic part was washed with brine (2×50 mL), dried and concentrated in vacuo to get a crude mass which was purified by Combi-Flash using a mixture of ethyl acetate and hexane as gradient eluent to get pure (1-naphthalen-1-yl-cyclopentyl)-acetonitrile (342) (710 mg, 44%) as a yellow gummy liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045486B2
Source datasetuspto-grants-2015_06
ORD IDord-63fbbb5efd294733a06b95a2a2c166ae
Source noteuspto-grants-2015_06