HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Acetoxycyclohexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 2-Cyclohexen-1-one | HCID 13594 | 41% |
| Product | 3-Acetoxycyclohexene | HCID 11116148 | 43% |
Reaction Steps
The reaction was conducted in the same manner as Example C1 except that acetic acid was employed for acetonitrile and the reaction temperature was set at 90° C. As a result, cyclohexene was transformed into 2-cyclohexen-1-one (cyclohexene-based selectivity 43%, yield 41%) and 1-acetyloxy-2-cyclohexene (cyclohexene-based selectivity 45%, yield 43%) with a transformation rate of 95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05958821 |
| Source dataset | uspto-grants-1999_09 |
| ORD ID | ord-e106e68b160a4fdcb9c639d8083e82e5 |
| Source note | uspto-grants-1999_09 |