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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3,5-Dinitrobenzoyl chloride | HCID 7432 | — |
| 반응물 | (1R)-1-[2-(2,4-difluorophenyl)-2-oxiranyl]ethanol | HCID 15130436 | — |
| 용매 | Trimethylamine | HCID 1146 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | [(1R)-1-[(2R)-2-(2,4-Difluorophenyl)-2-oxiranyl]ethyl]3,5-dinitrobenzoate | HCID 10691998 | 46.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06362206B1 |
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| 출처 데이터셋 | uspto-grants-2002_03 |
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| ORD ID | ord-80f214634efa4594864ccfbb47b83c3a |
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| 출처 메모 | uspto-grants-2002_03 |
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