Benzylamine → 4-(Benzylamino)butanenitrile
반응식
[CH2:1]([NH2:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br[CH2:10][CH2:11][CH2:12][C:13]#[N:14].C1CCCCC1.Br.C(N)C1C=CC=CC=1>C(OCC)C>[CH2:1]([NH:8][CH2:10][CH2:11][CH2:12][C:13]#[N:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
6
실험 절차
32.2 g of benzylamine, 14.8 g of 4-bromobutyronitrile and 30 ml of cyclohexane are stirred at room temperature for 12 hours. After the addition of diethyl ether the separated benzylamine hydrobromide is filtered off; the ether phase is washed with water, dried and concentrated by evaporation. The residue is distilled in vacuo to yield 11.5 g (66% of theory) of 4-benzylaminobutyronitrile (B.P. 114° to 120°/0.05 mm Hg).
후처리
- filtrationis filtered off
- washthe ether phase is washed with water
- customdried
- concentrationconcentrated by evaporation
- distillationThe residue is distilled in vacuo
출처 및 근거
- ORD 기록
- ord-3d7c63796250464c962ef37264c77f02
- 출처 데이터셋
- uspto-grants-1981_01
- 특허 번호
- US04243678
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