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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 279157생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/279157

반응식

참여 물질

역할이름HCID투입량
반응물3,5-Dinitrobenzoyl chlorideHCID 7432—
반응물(1R)-1-[2-(2,4-difluorophenyl)-2-oxiranyl]ethanolHCID 15130436—
용매TrimethylamineHCID 1146—
용매DichloromethaneHCID 6344—
생성물[(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoateHCID 1069199846.3%

반응 단계

(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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06362206B1
출처 데이터셋uspto-grants-2002_03
ORD IDord-80f214634efa4594864ccfbb47b83c3a
출처 메모uspto-grants-2002_03