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HRID 907595作成日:2026年10月26日

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

https://huagongshe.com/reaction/907595

反応式

関与物質

役割名称HCID仕込み量
反応物Diethyl EtherHCID 3283—
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物2,6-DifluorobenzaldehydeHCID 136284—
反応物Methyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetateHCID 2734718—
溶媒DichloromethaneHCID 6344—
生成物2-Benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl esterHCID 6739200072%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08013186B2
出典データセットuspto-grants-2011_09
ORD IDord-0b3e65617c3441adb5a287a7522686e1
出典メモuspto-grants-2011_09