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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 31051생성일: 2026년 10월 25일

2-(Trifluoromethyl)oxirane → [(S)-5-(3,3,3-Trifluoro-2-hydroxy-propyl)-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/31051

반응식

참여 물질

역할이름HCID투입량
반응물2-(Trifluoromethyl)oxiraneHCID 520769—
반응물((S)-6-Oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-carbamic acid tert-butyl esterHCID 58972520—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물[(S)-5-(3,3,3-Trifluoro-2-hydroxy-propyl)-6-oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl]-carbamic acid tert-butyl esterHCID 5897248476%

반응 조건

온도90 °C

반응 단계

((S)-6-Oxo-6,7-dihydro-5H-dibenzo[b,d]azepin-7-yl)-carbamic acid tert-butyl ester (108 mg, 0.33 mmol) and 1,1,1-trifluoro-2,3-epoxypropane (762 mg, 6.7 mmol) were dissolved in DMF (2 ml) and heated to 90° C. for 4 h in a sealed tube. After addition of another 500 mg of 1,1,1-trifluoro-2,3-epoxypropane, heating was continued for 18 h. The mixture was diluted with ethyl acetate and water (10 ml each), separated and the aqueous phase extracted twice with each 10 ml ethyl acetate. The combine organic phases are dried over magnesium sulfate and evaporated to dryness. Chromatography (silica, eluent heptanes/ethyl acetate gradient from 1 to 30%) afforded the title compound as white solid (76%). MS: m/e=437(M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07425551B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-fd4c0dd8cdad42c99f8b14c94dda3323
출처 메모uspto-grants-2008_09