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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485138Generated: October 26, 2026

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

https://huagongshe.com/reaction/485138

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 numberUS04535186
Source datasetuspto-grants-1985_08
ORD IDord-7a9ac46021e444bab3c09bd8a8447e49
Source noteuspto-grants-1985_08