HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Peroxide → 2-Cyclohexen-1-one, 4-phenyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Chloroselenobenzene | HCID 21928 | — |
| Reactant | 4-Phenylcyclohexanone | HCID 78605 | — |
| Product | 2-Cyclohexen-1-one, 4-phenyl- | HCID 11062876 | — |
| Product | HCID 19705215 | HCID 19705215 | — |
Reaction Steps
The intermediate 3-methyl-4-phenylcyclohexanone is prepared, first by the reaction of 4-phenylcyclohexanone with phenylselenenyl chloride and aqueous 30% hydrogen peroxide, yielding 4-phenyl-2-cyclohexenone, and then the reaction of the cyclohexenone with 1.4M methyllithium and aqueous ammonium chloride, affording 3-methyl-4-phenylcyclohexanone. The cyclohexanone is then reacted with cyanoguanidine as previously described. Example 15 provides a detailed description of how this reaction is conducted.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712281 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-34f1eb1b5d4a48c482f577ea44f545e1 |
| Source note | uspto-grants-1998_01 |