戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 476202作成日:2026年10月26日

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

https://huagongshe.com/reaction/476202

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Ammonium ChlorideHCID 25517—
反応物1,1'-CarbonyldiimidazoleHCID 68263—
反応物Cinnamic AcidHCID 444539—
反応物Lithium HexamethyldisilazideHCID 2733832—
溶媒TetrahydrofuranHCID 8028—
生成物Ethyl-3-oxo-5-phenylpent-4-enoateHCID 1105312957%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08637674B2
出典データセットuspto-grants-2014_01
ORD IDord-63a8dc5c60cf45ba8f8ce65ff454c2f0
出典メモuspto-grants-2014_01