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HRID 1444557Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1444557

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 2-benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl ester. This crude product 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
PatentnummerUS07662849B2
Quelldatensatzuspto-grants-2010_02
ORD IDord-773dde0ccd3e4ccb8fd3db445e0f50ca
Quellennotizuspto-grants-2010_02