반응식
[CH2:1]([O:8][C:9](Cl)=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Br.[Br:13][CH2:14][CH2:15][CH2:16][NH2:17]>C(Cl)Cl.[OH-].[Na+]>[Br:13][CH2:14][CH2:15][CH2:16][NH:17][C:9](=[O:10])[O:8][CH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1참가 물질
5
실험 절차
Benzylchloroformate (8.6 ml, 60 mmol) was added to a stirred mixture of 3-bromopropylamine hydrobromide (6.6 g, 30 mmol) in methylene chloride (100 ml) and 3N sodium hydroxide solution (100 ml) at 0° C. After stirring two phase reaction mixture at room temperature for overnight, organic layer was separated and washed with water twice (30 ml×2). After drying with MgSO4, the volatile solvent was evaporated under reduced pressure. The residue was purified with silica gel column chromatography (EtOAc:Hx=1:4) to obtain desire compound (8.6 g, 98%) as colorless oil.
후처리
- customtwo phase reaction mixture at room temperature for overnight
- customorganic layer was separated
- washwashed with water twice (30 ml×2)
- dry with materialAfter drying with MgSO4
- customthe volatile solvent was evaporated under reduced pressure
- customThe residue was purified with silica gel column chromatography (EtOAc:Hx=1:4)
출처 및 근거
- ORD 기록
- ord-8d5f0cc8a2fd49aa9f4c3dc927ecccc8
- 출처 데이터셋
- uspto-grants-2014_11
- 특허 번호
- US08895558B2
연결된 노트
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