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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64981Generated: October 25, 2026

Cyclohexanone → (1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrile

https://huagongshe.com/reaction/64981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexanoneHCID 7967—
ReactantHexaneHCID 8058—
ReactantAmmonium ChlorideHCID 25517—
ReactantBenzeneacetonitrile, 4-methoxy-HCID 66031—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
Product(1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrileHCID 9899621—

Reaction Conditions

Temperature-70 °C

Reaction Steps

p-Methoxyphenylacetonitrile (50 gm, 0.3 mole) was added to dry tetrahydrofuran (250 ml) and the solution cooled to -70° C. under nitrogen. n-Butyl lithium in hexane (210 ml, 0.3 mole) was added dropwise, with stirring. The temperature was maintained below -50° C. and a yellow precipitate appeared. After the addition was complete, the reaction mixture was maintained below -50° C. for 30 minutes and cyclohexanone (35 ml, 0.3 mole) was added. After a further 45 minutes below -50° C. the temperature was allowed to rise to 0° C. and a saturated ammonium chloride solution was added. The layers were separated and the aqueous layer extracted with diethyl ether. The combined organic solution was washed with brine, dried over magnesium sulphate and evaporated. The product crystallized (25.2 gm, m.p. 125°-127° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04611078
Source datasetuspto-grants-1986_09
ORD IDord-53b0532ff7824926866cd13eab492272
Source noteuspto-grants-1986_09