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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1650951Generated: October 27, 2026

Acetone → 1-[1-(4-Chlorophenyl)cyclobutyl]-3-hydroxy-3-methylbutan-1-one oxime

https://huagongshe.com/reaction/1650951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantWaterHCID 962—
Reactant1-[1-(4-Chlorophenyl)cyclobutyl]ethanone oximeHCID 86743937—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product1-[1-(4-Chlorophenyl)cyclobutyl]-3-hydroxy-3-methylbutan-1-one oximeHCID 86743936—

Reaction Conditions

Temperature-5 °C

Reaction Steps

A 1.6M solution of butyllithium in hexane (55 ml) was added to a stirred solution of the 1-[1-(4-chlorophenyl)cyclobutyl]ethanone oxime (8.94 g) in dry tetrahydrofuran (120 ml) the temperature being maintained below 0° C. for 40 minutes. The mixture was cooled to -5° C. and acetone (2.67 ml) was added dropwise. The temperature of the reaction mixture was allowed to rise to ambient temperature over a period of 16 hours. The mixture was cooled to 10° C. and water (100 ml) was added and the resulting aqueous mixture was washed with ether. The aqueous layer was acidified with 5N sulphuric acid and an oil separated. The oil was dissolved in ether and the ether solution was washed with water, dried and evaporated to yield 1-[1-(4-chlorophenyl)cyclobutyl]-3-hydroxy-3-methylbutan-1-one oxime.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04925879
Source datasetuspto-grants-1990_05
ORD IDord-33505a82fe51429ebbd990bc579e2b9a
Source noteuspto-grants-1990_05