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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16999Generated: October 26, 2026

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

https://huagongshe.com/reaction/16999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant2,6-DifluorobenzaldehydeHCID 136284—
ReactantMethyl 2-{[(benzyloxy)carbonyl]amino}-2-(dimethyl phosphono)acetateHCID 2734718—
SolventDichloromethaneHCID 6344—
Product2-Benzyloxycarbonylamino-3-(2,6-difluorophenyl)acrylic acid methyl esterHCID 6739200072%

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737300B2
Source datasetuspto-grants-2010_06
ORD IDord-89180631de3845848ba7d90fd33d5500
Source noteuspto-grants-2010_06