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HRID 1985780Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1985780

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
Edukt1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Edukt2,6-DifluorobenzaldehydeHCID 136284—
EduktMethyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetateHCID 2734718—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl esterHCID 6739200072%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07547701B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-9b5e42db42e24d79b9485febe3fff070
Quellennotizuspto-grants-2009_06