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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 322932Erstellt: 24. Oktober 2026

Sodium hydride → methyl (E)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylate

https://huagongshe.com/de/reaction/322932

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt2,4-Bis(benzyloxy)benzaldehydeHCID 1809080—
EduktMethyl 2-benzamido-2-(dimethoxyphosphoryl)acetateHCID 14104867—
LösungsmittelTetrahydrofuranHCID 8028—
Produktmethyl (E)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylateHCID 22010495—
Produktmethyl (Z)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylateHCID 70223822—

Reaktionsschritte

A stirred solution of methyl benzoylamino(dimethoxyphosphoryl)acetate (4.25 g) in dry tetrahydrofuran (30 mL) is treated with sodium hydride (0.66 g, 60% dispersion in mineral oil) under nitrogen. After stirring for 15 minutes a solution of 2,4-dibenzyloxybenzaldehyde (4.74 g) in dry tetrahydrofuran (15 mL) is added dropwise. The reaction mixture is stirred at room temperature for 18 hours, evaporated and the residue partitioned between ethyl acetate (100 mL) and water (75 mL). The organic phase is washed with brine (50 mL), dried over magnesium sulphate and evaporated. The residual yellow oil is purified by flash chromatography on silica eluting with initially with dichloro-methane then with a mixture of dichloromethane and ethyl acetate (9:1 v/v). Fractions homogeneous in the required products are evaporated to give methyl (E)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)acrylate (1 g) as a yellow foam, and methyl (Z)-2-benzoylamino-3-(2,4-dibenzyloxyphenyl)-acrylate (1.6 g) as a yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211234B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-da2bc403b35c40529730b4aeab800d13
Quellennotizuspto-grants-2001_04