HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 3-Cyclohexen-1-ol, 3,5,5-trimethyl-, acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Beta-Isophorone | HCID 10108 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3,5,5-Trimethylcyclohex-3-en-1-ol | HCID 11275049 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-Cyclohexen-1-ol, 3,5,5-trimethyl-, acetate | HCID 90791 | — |
Reaction Steps
Prepared by reduction by means of sodium borohydride in methanol of β-isophorone [obtained according to J. Am. Chem. Soc., 63, 2308 (1941)] and subsequent acetylation of the obtained 3,5,5-trimethyl-cyclohex-3-en-1-ol by means of acetic anhydride in the presence of sodium acetate at 50°C during 20 hours.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03957061 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-922b687f25494d3e96e309647a6668cb |
| Source note | uspto-grants-1976_05 |