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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372180Generated: October 26, 2026

Tert-Butyl hypochlorite → 1,3-Cyclohexanedione, 2-chloro-2-(2-propenyl)-

https://huagongshe.com/reaction/372180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl hypochloriteHCID 521297—
Reactant2-Allyl-cyclohexane-1,3-dioneHCID 566005—
SolventMethanolHCID 887—
Product1,3-Cyclohexanedione, 2-chloro-2-(2-propenyl)-HCID 1222965591.1%

Reaction Steps

t-Butylhypochlorite (104.6 g, 0196 mol) was added dropwise to a solution of 2-allyl-1,3-cyclohexanedione (132 g, 0.87 mol) in 650 ml of methanol at 0° C. The temperature was not allowed to rise above 20° C. The methanol was removed at reduced pressure in a 40° water bath and the residual oil was taken up in benzene. The benzene solution was washed with 5 percent sodium thiosulfate (3 × 250 ml), 5 percent sodium bicarbonate (3 × 250 ml) and water (1 × 250 ml). Evaporation of the benzene gave 148 g (91 percent) of 2-chloro-2-allyl-1,3-cyclohexanedione as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04089889
Source datasetuspto-grants-1978_05
ORD IDord-627fc7ea24314ad29e2d13b180b033cd
Source noteuspto-grants-1978_05