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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257604Generated: October 30, 2026

1-Chloro-4-(chloromethyl)benzene → HCID 11076339, compound

https://huagongshe.com/reaction/257604

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Chloro-4-(chloromethyl)benzeneHCID 7723—
ReactantPotassium HydroxideHCID 14797—
ReactantDimedoneHCID 31358—
SolventWaterHCID 962—
ProductHCID 11076339HCID 1107633942%

Reaction Conditions

Temperature59 °C

Reaction Steps

449 g (3.21 mols) dimedone (5,5-dimethylcyclohexane-1,3-dione) were added to a solution of aqueous potassium hydroxide comprising 166 g of 85% potassium hydroxide (2.52 mols) in 700 ml of water. The mixture was then warmed and a clear orange solution was obtained at 47° C. The solution was then heated to 59° C. and 544 g (3.21 mols) molten 4-chlorobenzyl chloride were added over a period of 1 hour with further heating to 85° C. Heating was continued for a further 2.5 to 3 hours up to a temperature of 100° C. The mixture was then cooled, the solid product filtered off, washed with water and dried in a vacuum oven at 50° C. The crude solid (815 g) was then dissolved in 2,400 ml methanol at reflux and 200 ml water added to produce a permanent cloudiness. The mixture was then allowed to cool to room temperature overnight with stirring. The solid so obtained was filtered, washed with about 400 ml cold methanol and dried in a vacuum oven to produce 340 g 2-(4-chlorobenzyl)-5,5-dimethylcyclohexane-1,3-dione as a white solid, m.pt. 188°-190° C. Yield: 42%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05262543
Source datasetuspto-grants-1993_11
ORD IDord-6fb1466f1fec4b78ae1ec3d1149214dd
Source noteuspto-grants-1993_11