Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 356803Generated: October 25, 2026

Hydrochloric Acid → 1,3-Diacetoxy-2-(2,4-difluorophenyl)-2-propanol

https://huagongshe.com/reaction/356803

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-Bromo-2,4-difluorobenzeneHCID 67674—
Reactant1,3-DiacetoxyacetoneHCID 243418—
ReactantMagnesiumHCID 5462224—
ReactantHCID 178505836HCID 178505836—
SolventTetrahydrofuranHCID 8028—
Product1,3-Diacetoxy-2-(2,4-difluorophenyl)-2-propanolHCID 15463462—

Reaction Conditions

Temperature-30 °C

Reaction Steps

Under an atmosphere of argon, 850 ml of THF solution of 2,4-difluorophenylmagnesium bromide prepared from 202.6 g (1.05 mol) of 2,4-difluorobromobenzene and 26.7 g (1.1 mol) of magnesium turnings was added dropwise at -30° C. to 1.7 l of THF solution of 174 g (1.00 mol) of 1,3-diacetoxyacetone which was previously cooled to -30° C. After the resulting liquid was stirred at -60° C. for 2 hours, a temperature thereof was gradually raised to room temperature. Then, to the reaction mixture was added 1 l of 1.2N aqueous solution of hydrochloric acid at 5° C. or below, and an aqueous layer was extracted twice with 1 l of ethyl acetate. The organic layer was washed with saturated aqueous solution of sodium chloride, dried and concentrated under reduced pressure to give 302 g of crude oil. The obtained oil was purified by means of column chromatography on silica gel (hexane:ethyl acetate=1:1) to give 125 g of the desired compound. The compound was recrystallized from toluene/hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05840553
Source datasetuspto-grants-1998_11
ORD IDord-482eb7ee2b7d4fa4af568fab801c7ce8
Source noteuspto-grants-1998_11