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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1447648Generated: November 1, 2026

Bromine → HCID 12870627, compound

https://huagongshe.com/reaction/1447648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantHCID 12870629HCID 12870629—
SolventCarbon TetrachlorideHCID 5943—
ProductHCID 12870627HCID 1287062799.3%

Reaction Steps

The ketone (20.0 g; 0.084 mole) was dissolved in carbontetrachloride (200 ml). The solution was cooled on ice and a 10% solution of bromine (0.084 mole) in CCl4 was added at such a rate that the drops were decolourized immediately. The total time of bromination was about 2 hours. After evaporation of the solvent in vacuo a pure oil of 2-bromo-5,5-dimethyl-6-(4-chlorophenyl)-3-hexanone (26.5 g; 99% yield) was obtained. To a solution of the bromoketone (5.0 g; 0.016 mole) in dimethylformamide (20 ml) was added potassium phtalimide (3.2 g; 0.017 mole) in portions under stirring during 5 minutes. The temperature was raised spontaneously to 40° C. Stirring was continued for 15 minutes. Chloroform (30 ml) was added and the mixture was poured into water (100 ml) under stirring. The organic layer was separated and the aqueous phase was washed with CHCl3. The combined chloroform phase was washed with 0.2 N sodium hydroxide solution and water. After drying over anhydrous sodium sulphate and evaporation of the solvent a yellow oil was obtained. The oil crystallized from ethanol-ether affording white crystals of 6-(4-chlorophenyl)-5,5-dimethyl-2-phtalimido-3-hexanone (2.6 g; 43% yield) melting at 96°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04177291
Source datasetuspto-grants-1979_12
ORD IDord-0219c64eec884e52b8bc1e6b0a6b9a28
Source noteuspto-grants-1979_12