Acrylonitrile → 4-Cyano-2-diaminomethylene-butyric acid ethyl ester
반응식
Cl.[CH2:2]([O:4][C:5](=[O:10])[CH:6]=[C:7]([NH2:9])[NH2:8])[CH3:3].C(N(CC)CC)C.[C:18](#[N:21])[CH:19]=[CH2:20]>O1CCCC1>[CH2:2]([O:4][C:5](=[O:10])[C:6]([CH2:20][CH2:19][C:18]#[N:21])=[C:7]([NH2:9])[NH2:8])[CH3:3]참가 물질
5
실험 절차
The resulting 3,3-diamino-acrylic acid ethyl ester hydrochloride (2.2 g, 13.2 mmol) was suspended in tetrahydrofuran (40 mL), triethylamine (2 mL, 14.3 mmol) and acrylonitrile (1.2 mL, 19.3 mmol) were added thereto, and the solution was refluxed for 6 hours. After the reaction was completed, the resulting triethylamine hydrochloride was filtered, and the filtrate was concentrated to obtain the title compound (0.6 g, 3.3 mmol, 25%).
후처리
- temperaturethe solution was refluxed for 6 hours
- filtrationthe resulting triethylamine hydrochloride was filtered
- concentrationthe filtrate was concentrated
출처 및 근거
- ORD 기록
- ord-c7c9ccec28754008a4a0fb919cbcca90
- 출처 데이터셋
- uspto-grants-2011_04
- 특허 번호
- US07932272B2
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