Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 596522Generated: October 30, 2026

Isopropenyl acetate → 2-(2-Oxopropyl)cyclohexanone

https://huagongshe.com/reaction/596522

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropenyl acetateHCID 7916—
ReactantAcetic AnhydrideHCID 7918—
ReactantCyclohexanoneHCID 7967—
ReactantPotassium PermanganateHCID 516875—
ReactantPotassium AcetateHCID 517044—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product2-(2-Oxopropyl)cyclohexanoneHCID 538581—

Reaction Conditions

Temperature70 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04011239
Source datasetuspto-grants-1977_03
ORD IDord-5a557faaa3574d00ab4bb4fd7e7eef61
Source noteuspto-grants-1977_03