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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 225409생성일: 2026년 10월 25일

Triethylamine → 2,3,5,6-Tetrafluorophenyl 3-[N-(9-fluorenylmethoxycarbonyl)]aminopropionate

https://huagongshe.com/reaction/225409

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물N-((9H-Fluoren-9-ylmethoxy)carbonyl)-L-alanineHCID 6364642—
반응물2,3,5,6-Tetrafluorophenyl trifluoroacetateHCID 15334258—
용매DichloromethaneHCID 6344—
생성물2,3,5,6-Tetrafluorophenyl 3-[N-(9-fluorenylmethoxycarbonyl)]aminopropionateHCID 22492770—

반응 단계

2,3,5,6-Tetrafluorophenyl trifluoroacetate (1.7 g, 6.5 mmol) was added dropwise to a solution of FMOC-alanine (2.0 g, 6.4 mmol) and triethylamine (1.0 ml, 7 mmol) in 20 ml of anhydrous CH2Cl2. After 1 hr., CH2Cl2 was removed by evaporation at reduced pressure using rotary evaporator, redissolved in 30 ml ethylacetate/hexane (1:1). Flash chromatography (4×20 cm, hexane/ethyl acetate, 3:1) afforded rude 4 as a white solid. It was recrystallized from hexane/ethyl acetate to give 4 as a white crystalline solid (2.3 g, 78%): 1H NMR (CDCl3, 200 MHz, ppm) 7.73 (d, 2H, J=7.1 Hz, aromatic protons), 7.75 (d, 2H, J=7.7 Hz, aromatic protons), 7.24-7.42 (m, 4H, aromatic protons), 7.01 (m, 1H, C6F4H), 5.21 (br s, 1H, —CONH—), 4.38 (d, 2H, J=7.1 Hz, —CH2OCO—), 4.20 (m, 1H, benzyl proton), 3.58 (m, -2H, NCH 2), 2.93 (t, 2H, J=5.4 Hz, —CH2CO—). Anal. Calcd. for C24H17NO4F4: C, 62.75; H, 3.73; N, 3.05. Found: C, 62.52; H, 3.59; N, 3.01.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07556923B1
출처 데이터셋uspto-grants-2009_07
ORD IDord-eeb8b18ee23347b8a7233bed4fc2aee4
출처 메모uspto-grants-2009_07