돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476202생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/476202

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Ammonium ChlorideHCID 25517—
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Cinnamic AcidHCID 444539—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매TetrahydrofuranHCID 8028—
생성물Ethyl-3-oxo-5-phenylpent-4-enoateHCID 1105312957%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637674B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-63a8dc5c60cf45ba8f8ce65ff454c2f0
출처 메모uspto-grants-2014_01