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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 532725Generated: October 26, 2026

Water → (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate

https://huagongshe.com/reaction/532725

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,1,3,3-TetramethylguanidineHCID 66460—
Reactant4-Chloro-3-FluorobenzaldehydeHCID 2724985—
ReactantMethyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetateHCID 86599651—
SolventDichloromethaneHCID 6344—
Product(Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylateHCID 6661795071.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

1,1,3,3-Tetramethylguanidine (2.11 ml, 16.8 mmol) was added to a 0° C. solution of methyl 2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)-acetate (5.00 g, 16.8 mmol) in DCM (70 mL). The reaction mixture was stirred at 0° C. for 30 minutes. Then a solution of 4-chloro-3-fluorobenzaldehyde (2.67 g, 16.8 mmol) in DCM (10 mL) was added by syringe. The reaction mixture was stirred for 10 minutes, then warmed to room temperature and stirred for another 1 hour. H2O was then added, and the mixture was extracted with DCM. The combined extracts were dried (Na2SO4), filtered, and concentrated. The resulting solids were recrystallized from IPA to give (Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylate (3.76 g, 67.8% yield) as a white powder (2 crops). LCMS (APCI−) m/z 328 [M−H]−.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08853199B2
Source datasetuspto-grants-2014_10
ORD IDord-30ebf75709f443d0bfb2518cd29498f0
Source noteuspto-grants-2014_10