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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 262075Generated: October 25, 2026

Mesityl oxide → 2,8-Dimethylnona-2,7-dien-4-one

https://huagongshe.com/reaction/262075

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMesityl oxideHCID 8858—
Reactant1-Chloro-3-methyl-2-buteneHCID 10429—
ReactantDiacetone AlcoholHCID 31256—
SolventAcetoneHCID 180—
Product2,8-Dimethylnona-2,7-dien-4-oneHCID 13244984—

Reaction Steps

Acetone under the reaction conditions forms also some diacetone alcohol and mesityl oxide, and these then react with the prenyl chloride to produce the above isomers of prenyl mesityl oxide, also called prenyl-substituted methyl pentenones, in the same manner as acetone reacts with prenyl chloride to produce methyl heptenone. It is also possible that prenyl chloride reacts with the diacetone alcohol in the same manner to give the corresponding hydroxy derivatives that subsequently dehydrate. The presence of such hydroxy ketones is observed in the residues of the methyl heptenone production by the process of U.S. Pat. No. 3,668,255.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04153633
Source datasetuspto-grants-1979_05
ORD IDord-5236353093b34b51b46c7a3bb94a86ea
Source noteuspto-grants-1979_05