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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16999생성일: 2026년 10월 26일

Diethyl Ether → 2-Benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl ester

https://huagongshe.com/reaction/16999

반응식

참여 물질

역할이름HCID투입량
반응물Diethyl EtherHCID 3283—
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물2,6-DifluorobenzaldehydeHCID 136284—
반응물Methyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetateHCID 2734718—
용매DichloromethaneHCID 6344—
생성물2-Benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl esterHCID 6739200072%

반응 단계

N-(Benzyloxycarbonyl)-α-phosphonoglycine trimethyl ester (Aldrich No. 37, 635-3; 6.7 g, 20 mmol) and 1,8-diazabicyclo[5,4,0]undec-7-ene (Aldrich No. 13, 900-9; 3.3 mL, 22 mmol) were dissolved in methylene chloride (11 mL) and stirred at room temperature for 15 min, and then cooled to <−30° C. A solution of 2,6-difluorobenzaldehyde (1.9 mL, 20 mmol) in methylene chloride (25 mL) was added to the reaction mixture dropwise over 20 min. The reaction mixture was stirred for another 20 min, and then allowed to warm up to room temperature for 30 min. The reaction mixture was then poured into ethyl ether (300 mL) and washed with 1 N HCl, brine and dried over MgSO4. Rotary evaporation gave crude 2-benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl ester which was purified by chromatography on a Medium Pressure Liquid Column (MPLC) eluting with 20% ethyl acetate/80% hexane to give pure product (5 g, 72% yield, liquid).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737300B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-89180631de3845848ba7d90fd33d5500
출처 메모uspto-grants-2010_06