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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989464Generated: October 30, 2026

Hydrochloric Acid → HCID 12113038, compound

https://huagongshe.com/reaction/989464

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantP-ChloroacetophenoneHCID 7467—
ReactantTrifluoroacetaldehydeHCID 65564—
Reactant1-Phenethylamine, (-)-HCID 75818—
CatalystZincchlorideHCID 3007855—
SolventTolueneHCID 1140—
ProductHCID 12113038HCID 1211303898.9%

Reaction Conditions

Temperature25.5 °C

Reaction Steps

At first, 5.5 g (40 mmol) of zinc chloride were added to a toluene solution (4 liters) containing 649 g (4.2 mol) of 4-chloroacetophenone (1b) as a ketone and 484 g (4.0 mol) of (S)-1-phenylethylamine ((S)-2a) as an optically active primary amine, followed by heating under reflux for 20 hr and by removing water (formed as a by-product) with a Dean-Stark tube during the reaction, in order to conduct the reaction. Then, 564 g (4.0 mol) of fluoral.ethylhemiacetal (4a) were dropped to the reaction liquid by spending 80 minutes at a temperature of not higher than 5° C., followed by stirring at 25-26° C. for 24 hr, thereby conducting the reaction. Then, 4-liter of 1N HCl were added to the reaction liquid, followed by stirring at room temperature for 1 hr, then washing with 2-liter of water, then concentration, and then vacuum drying, thereby obtaining 999 g of (R)-4,4,4-trifluoro-3-hydroxy-1-(4-chlorophenyl)-1-butanone ((R)-5ba, purity: 72%). Its optical purity was found to be 54% ee by the chiral HPLC as that of Example 1-30

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06639100B2
Source datasetuspto-grants-2003_10
ORD IDord-898fd2188bf742bda080001b5d702058
Source noteuspto-grants-2003_10