HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → 2-Phenyl-2-(2-cyanoethyl)-6-diazocyclohexanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | p-Toluenesulfonyl azide | HCID 13661 | — |
| Reactant | 2-Oxocyclohexanecarbaldehyde | HCID 12197585 | — |
| Reactant | 2-Phenyl-2-(2-cyanoethyl)-6-formylcyclohexanone | HCID 21330610 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 2-Phenyl-2-(2-cyanoethyl)-6-diazocyclohexanone | HCID 21330523 | — |
Reaction Steps
Reaction of a formyl cyclohexanone derivative with para-toluenesulfonylazide effects displacement of the formyl group by a diazo moiety to provide a diazocyclohexanone derivative. For example, a formyl cyclohexanone derivative such as 2-phenyl-2-(2-cyanoethyl)-6-formylcyclohexanone can be reacted with about an equimolar quantity of para-toluene-sulfonylazide in the presence of dimethylamine or diethylamine, in an organic solvent such as diethyl ether, to provide, for instance, 2-phenyl-2-(2-cyanoethyl)-6-diazocyclohexanone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04141893 |
| Source dataset | uspto-grants-1979_02 |
| ORD ID | ord-359c058491d84e17bb4f41b230e86d91 |
| Source note | uspto-grants-1979_02 |