Benzyl Bromide → N-Boc-N-benzyl-3-chloropropylamine

HRID 321948노트

반응식

HRID 321948 반응식
[C:1]([NH:8][CH2:9][CH2:10][CH2:11][Cl:12])([O:3][C:4]([CH3:7])([CH3:6])[CH3:5])=[O:2].[H-].[Na+].[CH2:15](Br)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C1COCC1.CCOCC.O>[C:1]([N:8]([CH2:9][CH2:10][CH2:11][Cl:12])[CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)([O:3][C:4]([CH3:5])([CH3:6])[CH3:7])=[O:2]

참가 물질

7

반응물 3

HCID 7498Benzyl BromideHCID 24758Sodium hydrideHCID 10932310N-Boc-3-Chloropropylamine

생성물 1

HCID 11098062N-Boc-N-benzyl-3-chloropropylamine수율 13.4%

시약·촉매·용매 3

HCID 962Water용매HCID 3283Diethyl Ether용매HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of N-Boc-3-chloropropylamine (10.0 g, 51.8 mmol) in THF was added sodium hydride (1.87 g, 78 mmol). After 20 min, benzyl bromide (9.24 mL, 78 mmol) was added and the reaction mixture was heated at reflux for 16 h. After cooling, the reaction mixture was diluted with Et2O (150 mL) and H2O (50 mL), the layers were separated and the aqueous layer was extracted twice with Et2O. The combined organic phases were washed with H2O and brine, dried (MgSO4), filtered and concentrated. The resulting yellow oil was purified by flash chromatography (SiO2, 10% EtOAc-hexane) to give N-Boc-N-benzyl-3-chloropropylamine (1.97 g, 13% yield) as a pale yellow oil.

후처리

  1. temperaturethe reaction mixture was heated
  2. temperatureat reflux for 16 h
  3. temperatureAfter cooling
  4. customthe layers were separated
  5. extractionthe aqueous layer was extracted twice with Et2O
  6. washThe combined organic phases were washed with H2O and brine
  7. dry with materialdried (MgSO4)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customThe resulting yellow oil was purified by flash chromatography (SiO2, 10% EtOAc-hexane)

출처 및 근거

ORD 기록
ord-256e366c627e4932a36fa4f2e340f0d0
출처 데이터셋
uspto-grants-2001_04
특허 번호
US06211170B1

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