반응식
[CH2:1]([NH2:7])[CH2:2][CH2:3][CH2:4][CH2:5][CH3:6].[CH2:8](Br)[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>>[CH2:8]([NH:7][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH3:6])[C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1참가 물질
3
실험 절차
A! 200 ml (1.49 moles) of hexylamine cooled to 5° C. were added with benzyl bromide (42.3 ml, 0.35 mole), and the resultant mixture was stirred for 1 hour at room temperature. The hexylamine in excess was then distilled off under vacuum, and the residue dissolved in 300 ml of ethyl ether and washed with 200 ml of 0.5N sodium hydroxide. The ether phase was anhydrified over sodium sulfate and evaporated to dryness thus yielding 75.5 g of a crude which, by distillation under vacuum, gave 59 g (yield: 89%) of N-benzyl-N-hexylamine (b.p.--90°-95° C./0.6 mmHg).
후처리
- distillationThe hexylamine in excess was then distilled off under vacuum
- dissolutionthe residue dissolved in 300 ml of ethyl ether
- washwashed with 200 ml of 0.5N sodium hydroxide
- customevaporated to dryness
- customthus yielding 75.5 g of a crude which
- distillationby distillation under vacuum
출처 및 근거
- ORD 기록
- ord-b52e3838c7d1473386d8e76d81f29a25
- 출처 데이터셋
- uspto-grants-1998_10
- 특허 번호
- US05827881
연결된 노트
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