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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36575Generated: October 30, 2026

Acetic Acid → 4-(5-Chloro-6-methylene-2,2-dimethylcyclohexyl)-2-butanone

https://huagongshe.com/reaction/36575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantDihydro-alpha-iononeHCID 35821—
ReactantMonobasic potassium phosphateHCID 516951—
ReactantSodium HypochloriteHCID 23665760—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product4-(5-Chloro-6-methylene-2,2-dimethylcyclohexyl)-2-butanoneHCID 19937284—

Reaction Steps

388 g (2 mol) of dihydro-α-ionone was placed in 2.2 l of methylene chloride in a 10 l four-necked flask fitted with a stirrer, thermometer, condenser and dropping funnel. Then, 660 g (4.6 mol) of potassium dihydrogen phosphate dissolved in 3 l of water was added and the resulting emulsion was cooled in an ice bath. 1.6 (2.3 mol) of sodium hypochlorite solution (~12%) was added at about 10° within 1.5 hours and, after about 3 hours at 15°, a further 350 ml (0.5 mol) was added. The pH value of the mixture was adjusted to ~5.5 with acetic acid and it was stirred at room temperature. After a total reaction time of 27 hours the phases were separated and the aqueous phase was extracted 4 times with methylene chloride. The combined organic phases were washed neutral once with water, twice with saturated NaHCO3 solution and a further 3 times with water, dried over MgSO4, filtered and evaporated (bath temperature=room temperature). 407.45 g 4-(3-chloro-2-methylidene-6,6-dimethyl-cyclohex-1-yl)-butan-2-one was obtained as a yellow liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05416069
Source datasetuspto-grants-1995_05
ORD IDord-b93882487f05419a874ba4229e8494b8
Source noteuspto-grants-1995_05