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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 279157Erstellt: 25. Oktober 2026

3,5-Dinitrobenzoyl chloride → [(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoate

https://huagongshe.com/reaction/279157

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3,5-Dinitrobenzoyl chlorideHCID 7432—
Edukt(1R)-1-[2-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 15130436—
LösungsmittelTrimethylamineHCID 1146—
LösungsmittelDichloromethaneHCID 6344—
Produkt[(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoateHCID 1069199846,3%

Reaktionsschritte

(1R)-1-[2-(2,4-Difluorophenyl)-2-oxiranyl]ethanol (31.5 g) and 3,5-dinitrobenzoyl chloride (40 g) were dissolved in methylene chloride (500 ml), to which trimethylamine (24.1 ml) was added dropwise at ice-bath temperature. After the mixture was stirred at room temperature for 3.5 hours, it was washed with water (150 ml) and 5% sodium bicarbonate aqueous solution successively, dried over magnesium sulfate and concentrated under reduced pressure. The precipitated crystals were filtrated and washed with methylene chloride. The mother liquor and the washings were combined and distilled off under reduced pressure. Ethyl acetate (25 ml) and methanol (300 ml) were added to the residue, and the mixture was cooled in an ice bath. The precipitated crystals were collected by filtration and recrystallized from a mixture of ethyl acetate (25 ml) and methanol (250 ml) to give [(1R)-1-[(2R)-2-(2,4-difluorophenyl)-2-oxiranyl]ethyl] 3,5-dinitrobenzoate (28.7 g) as colorless needles.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06362206B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-80f214634efa4594864ccfbb47b83c3a
Quellennotizuspto-grants-2002_03