HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065262Generated: October 29, 2026
O-Xylene → 1-(4-Fluorophenyl)-4-oxocyclohexanecarbonitrile
https://huagongshe.com/reaction/1065262
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Benzeneacetonitrile, 4-fluoro- | HCID 68016 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Product | 1-(4-Fluorophenyl)-4-oxocyclohexanecarbonitrile | HCID 91805 | — |
Reaction Steps
A mixture of 221 parts of 4-fluorobenzeneacetonitrile, 700 parts of sodium methoxide solution 30% and 900 parts of dimethylbenzene is stirred for 5 minutes. Then there are added dropwise 309 parts of methyl 2-propanoate (exothermic reaction: temperature rises to 65° C.). Upon completion, stirring is continued overnight at reflux temperature. The methanol is distilled off till an internal temperature of 110° C. is reached. After cooling, 1000 parts of a hydrochloric acid solution 6 N are added dropwise and the whole is stirred and refluxed for 5 minutes. Upon cooling, the layers are separated. The organic phase is dried, filtered and evaporated. The residue is stirred and refluxed for 4 hours together with 500 parts of acetic acid, 500 parts of water and 500 parts of a hydrochloric acid solution. After cooling, the product is extracted with trichloromethane. The extract is washed successively with water, with a diluted sodium hydroxide solution and again with water till neutralization, dried, filtered and evaporated. The residue is crystallized from 2-propanol, yielding 134.5 parts of 1-(4-fluorophenyl)-4-oxocyclohexanecarbonitrile; mp. 91.8° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04329353 |
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| Source dataset | uspto-grants-1982_05 |
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| ORD ID | ord-8d5d265155b242bb800df69ca407028f |
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| Source note | uspto-grants-1982_05 |
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