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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 984934Erstellt: 25. Oktober 2026

Ethyl Acetate → HCID 21907868, Verbindung

https://huagongshe.com/reaction/984934

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktSodium hydrideHCID 24758—
Edukt4,4'-DibromobenzophenoneHCID 72868—
LösungsmittelHydrochloric AcidHCID 313—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 21907868HCID 2190786899%

Reaktionsschritte

A solution of triethyl phosphonoacetate (26.8 g, 120.0 mmol) in dry THF (100 mL) was added at 0° C. over a period of 25 min. to a stirred suspension of sodium hydride (60% in oil, 4.8 g, 120.0 mmol) in dry THF (100 ml). After stirring at 0° C. for 30 min. a solution of 4,4′-dibromobenzophenone (20.4 g, 60.0 mmol) in dry THF (200 ml) was added and the mixture slowly warmed to room temperature, and stirring continued for 48 h. The reaction mixture was diluted with 1N hydrochloric acid (400 ml) and ethyl acetate (100 ml). The organic phase was separated, and the aqueous phase further extracted with ethyl acetate (2×300 ml). The combined organic phases were washed with water (300 ml×3), dried (MgSO4), filtered and concentrated in vacuo. The product was purified by column chromatography on silica gel (15% ethyl acetate in n-heptane eluent) to give 24.5 g (99%) 3,3-bis-(4-bromophenyl)-acrylic acid ethyl ester as an off-white amorphous solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06869967B2
Quelldatensatzuspto-grants-2005_03
ORD IDord-9d27f9bb31a14003a8d16fa5f67e36ef
Quellennotizuspto-grants-2005_03