HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1060261Generated: October 30, 2026
Acetonitrile → Acetonitrile, cyclohexylidene-
https://huagongshe.com/reaction/1060261
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Hexane | HCID 8058 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Solvent | Water | HCID 962 | — |
| Product | Acetonitrile, cyclohexylidene- | HCID 97105 | — |
Reaction Steps
A 10 l round-bottom flask is loaded with 285 g (4.57 mols) of 90% potassium hydroxide in flakes and 1775 ml of hexane. The mixture is heated to 55° C. and, keeping heating, a solution consisting of 450 g (4.59 mols) of cyclohexanone and 1351 ml of acetonitrile is quickly dropped therein (during the addition temperature falls to 52.6° C.). The mixture is refluxed for 7 hours, then cooled at room temperature. 2863 ml of water are added thereof to dissolve the solid. The organic phase is washed twice with water (1000 ml each). The phases are separated and the organic phase is evaporated to dryness under vacuum, to obtain 462 g of a residue which is distilled under 10 mmHg at 100-105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06521788B2 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-4103d33773a84c1f9fe0d0933d852729 |
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| Source note | uspto-grants-2003_02 |
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