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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132582생성일: 2026년 10월 26일

Acetic Anhydride → N-{4-Fluoro-2-[(2S)-oxiran-2-ylmethoxy]phenyl}acetamide

https://huagongshe.com/reaction/132582

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AnhydrideHCID 7918—
반응물DiisopropylethylamineHCID 81531—
반응물(2S)-2-[(5-Fluoro-2-nitrophenoxy)methyl]oxiraneHCID 28109166—
반응물HCID 178418361HCID 178418361—
촉매PlatinumHCID 23939—
용매Ethyl AcetateHCID 8857—
생성물N-{4-Fluoro-2-[(2S)-oxiran-2-ylmethoxy]phenyl}acetamideHCID 2080654861.3%

반응 단계

(2S)-2-[(5-fluoro-2-nitrophenoxy)methyl]oxirane (0.32 g, 1.5 mmol) was dissolved in ethyl acetate (40 ml). Platinum on charcoal (0.15 g) was added, and the mixture was stirred in the atmosphere of hydrogen for 3 h at room temperature and atmospheric pressure. The catalyst was filtered and washed on the filter with ethyl acetate (10 ml). Acetic anhydride (0.31 g, 0.28 ml, 3 mmol) and ethyldi(i-propyl)amine (0.39 g, 0.52 ml, 3 mmol) were added to the solution. The reaction mixture was stirred at room temperature for 3 h, then washed with 1M sodium hydroxide (NaOH) (30 ml) and brine (30 ml), and dried with sodium sulphate (Na2SO4). Evaporation of the solvent and flash chromatography on silica gel with n-heptane/ethyl acetate (from 25 to 75%) afforded the subtitle compound (0.21 g, 0.92 mmol, 61%) as a colourless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388020B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-f285811dac3e41b995ef2461e620a5c0
출처 메모uspto-grants-2008_06