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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279157Generated: October 26, 2026

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

https://huagongshe.com/reaction/279157

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dinitrobenzoyl chlorideHCID 7432—
Reactant(1R)-1-[2-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 15130436—
SolventTrimethylamineHCID 1146—
SolventDichloromethaneHCID 6344—
Product[(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoateHCID 1069199846.3%

Reaction Steps

(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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06362206B1
Source datasetuspto-grants-2002_03
ORD IDord-80f214634efa4594864ccfbb47b83c3a
Source noteuspto-grants-2002_03