HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Acetoxycyclohexene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrogen Peroxide | HCID 784 | — |
| Reactant | Cyclohexene | HCID 8079 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Product | 3-Acetoxycyclohexene | HCID 11116148 | 50% |
Reaction Steps
A 500 ml three-neck flask was charged with 15 g of cyclohexene (0.18 moles), 150 g of acetic acid and 80 mg of palladium acetate (0.36 mmoles). The temperature was taken to 50°, and then 10.6 g (0.22 moles) of 70% by weight hydrogen peroxide were introduced in 8 h. The reaction was continued for 2 more hours, while keeping the temperature at 50°. The acetic acid was then distilled (35°, 20×102Pa). The residue was distilled under vacuum (64°-68°, 15×102Pa) to provide cyclohex-2-en-1-yl acetate, 90% pure (13 g, yield 50%). cyclohex-2-en-1-yl-acetate
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05554786 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-71a1b52b81d44cfc915494adac8c282e |
| Source note | uspto-grants-1996_09 |