반응식
[O:1]=[C:2]([CH2:8][C:9](=[O:11])[CH3:10])[C:3]([O:5][CH2:6][CH3:7])=[O:4].C(OCC)(OCC)O[CH2:14][CH3:15].[Cl-].[NH4+]>C(O)C>[CH2:14]([O:11][C:9]([CH3:10])=[CH:8][C:2](=[O:1])[C:3]([O:5][CH2:6][CH3:7])=[O:4])[CH3:15]참가 물질
5
실험 절차
To a stirred solution of ethyl 2,4-dioxopentanoate (36.5 g, 231 mmol) and triethyl orthoformate (41 mL, 246 mmol) in ethanol (60 mL) was added ammonium chloride (3.7 g, 69 mmol). The suspension was stirred at RT overnight. LCMS showed that the reaction was mostly complete. (Hydrolyzes on LCMS to some degree?) The reaction was concentrated under vacuum. The remaining oil was taken up in Et2O (300 mL), filtered to remove insolubles, rinsed with Et2O, and concentrated under vacuum. The product was obtained by short path distillation under vacuum (bp 70 to 77° C. at 0.09 mmHg) to give the product ethyl 4-ethoxy-2-oxopent-3-enoate (36.5 g, 47.3 mmol, 79% yield) as a light yellow oil.
후처리
- concentration) The reaction was concentrated under vacuum
- filtrationfiltered
- customto remove insolubles
- washrinsed with Et2O
- concentrationconcentrated under vacuum
- customThe product was obtained by short path distillation under vacuum (bp 70 to 77° C. at 0.09 mmHg)
출처 및 근거
- ORD 기록
- ord-b160e798a785465a9a8987f6922ce044
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08536179B2
연결된 노트
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