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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112342Generated: October 26, 2026

Mesityl oxide → 6-Methyl-3-(propan-2-ylidene)hept-5-en-2-one

https://huagongshe.com/reaction/1112342

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMesityl oxideHCID 8858—
Reactant1-Chloro-3-methyl-2-buteneHCID 10429—
ReactantSodium HydroxideHCID 14798—
Reactant18,18-Dimethylnonadecylazanium chlorideHCID 53249239—
SolventWaterHCID 962—
Product6-Methyl-3-(propan-2-ylidene)hept-5-en-2-oneHCID 13244983—

Reaction Steps

To a solution of 600 g of sodium hydroxide in 490 g of water was added 980 g of mesityl oxide together with 520 g of prenyl chloride and 25 g of trimethylstearylammonium chloride, and the mixture was reacted in a water bath under stirring for 2 hours (The reaction temperature rose to 70° C.). The reaction mixture was poured into water and extracted with ethyl ether. The ethereal solution was washed with water and dried over anhydrous sodium sulfate. The ether was distilled off under reduced pressure and the residue (1250 g) was further distilled to recover the unreacted mesityl oxide. Thereupon, as higher-boiling products, 560 g of a 2.5:1 mixture of 3-isopropenyl-6-methyl-5-hepten-2-one and 3-isopropylidene-6-methyl-5-hepten-2-one (purity 96.4%) was obtained. Based on the purity of 83.71% for the prenyl chloride used, the yield of 3-isopropenyl-6-methyl-5-hepten-2-one was 59% (410 g) and that of 3-isopropylidene- 6-methyl-5-hepten-2-one was 19% (130 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04122119
Source datasetuspto-grants-1978_10
ORD IDord-f51c7aaddf9b4be6bba4413ca3545ffb
Source noteuspto-grants-1978_10