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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 476202Erstellt: 24. Oktober 2026

Ethyl Acetate → Ethyl-3-oxo-5-phenylpent-4-enoate

https://huagongshe.com/de/reaction/476202

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktAmmonium ChlorideHCID 25517—
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktCinnamic AcidHCID 444539—
EduktLithium HexamethyldisilazideHCID 2733832—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktEthyl-3-oxo-5-phenylpent-4-enoateHCID 1105312957%

Reaktionsschritte

Trans-cinnamic acid (5 mmol, manufactured by Fluka), 1,1′-carbonyl diimidazole (892 mg, 5.5 mmol, manufactured by Aldrich) and tetrahydrofuran (10 mL) were charged in a 25 mL round-bottom flask, followed by stirring at room temperature for 1 hour. 1M lithium bis(trimethylsilyl)amide (10 mL, 10 mmol, manufactured by Aldrich), ethyl acetate (977 μL, 10 mmol), and tetrahydrofuran (10 mL) were added to thereto, followed by stirring at −78° C. for 1 hour. Two solutions were mixed, gradually warmed and stirred at room temperature for 1 hour. A saturated ammonium chloride aqueous solution (50 mL) and ethyl acetate (50 mL) were added thereto, followed by separation of layers into two layers and washing with distilled water and saline. The organic layer was dried over anhydrous sodium sulfate and separated by column chromatography (n-Hex/EtOAc=15/1 (v/v)) to afford Compound 8a.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637674B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-63a8dc5c60cf45ba8f8ce65ff454c2f0
Quellennotizuspto-grants-2014_01