HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyclohexanone → 1-Aminocyclohexanecarbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Sodium Cyanide | HCID 8929 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-Aminocyclohexanecarbonitrile | HCID 79635 | 89.6% |
Reaction Steps
1.23 g of sodium cyanide, 1.58 g of ammonium chloride and 8 ml of ammonium hydroxide are introduced, the whole is taken to 0° C. and 2.1 g of cyclohexanone is added. The reaction medium is left to return to ambient temperature under agitation for 18 hours, diluted in a small amount of water and decanted. The aqueous phase is extracted with methylene chloride, the organic phases are combined, washed with salt water, dried, filtered and concentrated. In this way 2.38 g of expected product (colourless oil) is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06087509 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-760aa3e0bcd842e5aa262a391e842d4b |
| Source note | uspto-grants-2000_07 |