HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 14631299, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Cyclohexanone, 4-hydroxy-2,2,6-trimethyl-, (4R,6R)- | HCID 10313234 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 14631299 | HCID 14631299 | 99.4% |
Reaction Steps
300 g of (4R, 6R)-4-hydroxy-2,2,6-trimethylcyclohexanone were dissolved in 154.7 ml of pyridine. The solution was treated dropwise at -3° C. to 0° C. within 10 minutes with 1.2 l of acetic anhydride and then stirred at room temperature for a further 4.25 hours. The reaction mixture was subsequently concentrated on a rotary evaporator at 60° C./16 mbar, whereby there were obtained 394.7 g of crude product as a yellow oil. Distillation of the crude product gave at about 95° C./0.07 mbar 378.4 g (99.4%) of (4R, 6R)-4-acetoxy-2,2,6-trimethylcyclohexanone as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05227507 |
| Source dataset | uspto-grants-1993_07 |
| ORD ID | ord-5e21179d959342439294bf0e246e2ba0 |
| Source note | uspto-grants-1993_07 |