HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596522Generated: October 30, 2026
Isopropenyl acetate → 2-(2-Oxopropyl)cyclohexanone
https://huagongshe.com/reaction/596522
Participants
| Role | Name | HCID | Charge |
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| Reactant | Isopropenyl acetate | HCID 7916 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Cyclohexanone | HCID 7967 | — |
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-Oxopropyl)cyclohexanone | HCID 538581 | — |
Reaction Steps
To a solution of manganic acetate in acetic acid, prepared in situ by the addition of 16 g. of potassium permanganate (0.1 m.) to 88 g. of manganous acetate dihydrate (Mn(OAc)2. 2H2O) (0.42 m.) in 570 milliliters of glacial acetic acid followed by 124 ml. of acetic anhydride and 60 g. of potassium acetate, were added 100 g. (1.0 m.) of isopropenyl acetate and 98 g. (1.0 m.) of cyclohexanone. The reaction mixture was heated under nitrogen to 70° C. until the brown manganic color disappeared. The reaction mixture was cooled, diluted with water, and extracted with ether. The product, 2-acetonyl-cyclohexanone ##STR84## was isolated by distillation, b.p. 70° C. at 0.05 mm. mercury, yield about 8 g. (20% based on Mn).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04011239 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-5a557faaa3574d00ab4bb4fd7e7eef61 |
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| Source note | uspto-grants-1977_03 |
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