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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 82355Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/82355

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1,1,3,3-TetramethylguanidineHCID 66460—
Edukt4-Chloro-3-FluorobenzaldehydeHCID 2724985—
EduktMethyl2-(tert-butoxycarbonyl)-2-(dimethoxyphosphoryl)acetateHCID 86599651—
LösungsmittelDichloromethaneHCID 6344—
Produkt(Z)-methyl 2-(tert-butoxycarbonyl)-3-(4-chloro-3-fluorophenyl)acrylateHCID 6661795071,1%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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 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 and then warmed to room temperature with continued stirring for 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]−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846681B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-d870addbf84d4f418593ae6d602956dc
Quellennotizuspto-grants-2014_09