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HRID 356804Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/356804

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
Edukt1-Bromo-2,4-difluorobenzeneHCID 67674—
Edukt1,3-DiacetoxyacetoneHCID 243418—
EduktButyllithiumHCID 178418339—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelHexaneHCID 8058—
Produkt1,3-Diacetoxy-2-(2,4-difluorophenyl)-2-propanolHCID 1546346227,8%

Reaktionsbedingungen

Temperatur-30 °C

Reaktionsschritte

Under an atmosphere of argon, 22.5 g of 2,4-difluorobromobenzene was dissolved in 200 ml of diethyl ether and to the resulting solution was added dropwise 73 ml of 1.63M n-hexane solution of n-butyllithium at -30° C. The resulting liquid was stirred for 1 hour and stored at -60° C. This liquid was carefully added dropwise using an injection cylinge to 150 ml of diethyl ether solution of 17.4 g 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, the reaction mixture was transferred to 100 ml of 1.2N aqueous solution of hydrochloric acid at 5° C. or below, and the organic layer was separated therefrom and the aqueous layer was extracted twice with 100 ml of ethyl acetate. The organic layers were combined and washed with saturated aqueous solution with sodium chloride, dried over anhydrous magnesium sulfate. The resulting organic layer was filtered and the solvent was removed under reduced pressure. Thus obtained concentrate was purified by column chromatography on silica gel (hexane:ethyl acetate=1:1) to give 8 g of the desired compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05840553
Quelldatensatzuspto-grants-1998_11
ORD IDord-a713d00dc68e43c09564a26011c02dd8
Quellennotizuspto-grants-1998_11