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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086840Generated: October 31, 2026

Sulfuric Acid → HCID 19818530, compound

https://huagongshe.com/reaction/1086840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantDiisopropylamineHCID 7912—
ReactantHexafluoroacetoneHCID 12695—
ReactantEthanone, 1-(3,4-dichlorophenyl)-HCID 75841—
ReactantLithium diisopropylamideHCID 2724682—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 19818530HCID 19818530—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A solution of 3,4-dichloroacetophenone (5.0 g.)in tetrahydrofuran (50 ml.) was added dropwise to a stirred solution of lithium diisopropylamide (prepared from n-butyl-lithium [19.8 ml. of a 1.6 molar solution in hexane] and diisopropylamine (4.3 ml.) in tetrahydrofuran (200 ml.) during 10 minutes at 0° C.) which was cooled to -78° C., and the mixture was stirred at -78° C. for 30 minutes and then at -50° C. for 45 minutes, and then recooled to -78° C. Anhydrous hexafluoroacetone (10 ml., generated by treating the sesquihydrate with concentrated sulphuric acid) was distilled into the mixture, which was then stirred for 1 hour at -78° C. Methanol (10 ml.) and saturated aqueous ammonium chloride solution (50 ml.) were added, the mixture was allowed to warm up to laboratory temperature and was poured into water (250 ml.) and the mixture was extracted with diethyl ether. The extract was washed with saturated aqueous sodium chloride solution, dried over magnesium sulphate and evaporated to dryness under reduced pressure, and there was thus obtained as an oil 1-(3,4-dichlorophenyl)-4,4,4-trifluoro-3-hydroxy-3-trifluoromethylbutan-1-one which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05032592
Source datasetuspto-grants-1991_07
ORD IDord-55b7b1a662914b62bef26c6a1f938742
Source noteuspto-grants-1991_07