HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64981Generated: October 25, 2026
Cyclohexanone → (1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrile
https://huagongshe.com/reaction/64981
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Benzeneacetonitrile, 4-methoxy- | HCID 66031 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1-Hydroxycyclohexyl)(4-methoxyphenyl)acetonitrile | HCID 9899621 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04611078 |
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| Source dataset | uspto-grants-1986_09 |
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| ORD ID | ord-53b0532ff7824926866cd13eab492272 |
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| Source note | uspto-grants-1986_09 |
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