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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 19177생성일: 2026년 10월 25일

Ammonium Chloride → 2-(Benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl ester

https://huagongshe.com/reaction/19177

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물Ethyl 2-(diphenylmethyleneamino)acetateHCID 319508—
반응물Potassium tert-butoxideHCID 23665647—
반응물Trifluoro-methanesulfonic acid 1-fluoro-cyclopentylmethyl esterHCID 86635233—
용매DimethylformamideHCID 6228—
생성물2-(Benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl esterHCID 8663523458%

반응 단계

To a solution of N-(diphenylmethylene)glycine ethyl ester (1.94 g, 7.26 mmol) in N,N-dimethylformamide (10 mL) at 0° C. was added solid potassium t-butoxide (0.89 g, 7.93 mmol) over 10 min and the resulting solution stirred for an additional 15 min. A trifluoro-methanesulfonic acid 1-fluoro-cyclopentylmethyl ester (2 g, 7.99 mmol) solution in N,N-dimethylformamide (2 mL) was added and the resulting mixture allowed to warm to room temperature over 2 h. The resulting mixture was poured into saturated ammonium chloride and extracted with dichloromethane (200 mL). The organic phase was separated, washed with saturated sodium chloride solution and dried over magnesium sulfate. The mixture was filtered and evaporated and the residue purified by AnaLogix flash chromatography (AnaLogix SuperFlash Flash Column 120 g, 10% to 20% ethyl acetate/hexanes) which afforded 2-(benzhydrylidene-amino)-3-(1-fluoro-cyclopentyl)-propionic acid ethyl ester (1.36 g, 58%) as a yellow oil: 1H NMR (300 MHz, CDCl3) δ ppm 1.26 (t, J=7.1 Hz, 3H), 1.39-1.97 (m, 8H), 2.11-2.41 (m, 1H), 2.45-2.76 (m, 1H), 4.01-4.27 (m, 2H), 4.37 (dd, J=7.5, 4.5 Hz, 1H), 7.16-7.25 (m, 2H), 7.29-7.41 (m, 3H), 7.41-7.56 (m, 3H), 7.64 (d, J=7.8 Hz, 2H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741327B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-88643da42a2d4fc7b2df92278bd8a00b
출처 메모uspto-grants-2010_06