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Ammonium Hydroxide → 1-(6-Chloropyridin-3-yl)ethan-1-amine

HRID 1640884
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HRID 1640884 반응식
[BH4-].[Na+].[Cl:3][C:4]1[N:9]=[CH:8][C:7]([C:10](=[N:12]O)[CH3:11])=[CH:6][CH:5]=1.[OH-].[NH4+]>COCCOC.[Ti](Cl)(Cl)(Cl)Cl>[Cl:3][C:4]1[N:9]=[CH:8][C:7]([CH:10]([NH2:12])[CH3:11])=[CH:6][CH:5]=1
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참가 물질

6

반응물 3

HCID 14923Ammonium HydroxideHCID 4311764Sodium borohydrideHCID 53396275HCID 53396275, 화합물

생성물 1

HCID 157456051-(6-Chloropyridin-3-yl)ethan-1-amine수율 38.3%

시약·촉매·용매 2

HCID 24193Titanium Tetrachloride촉매HCID 80711,2-Dimethoxyethane
용매

실험 절차

Cool a solution of sodium borohydride (2.96 g, 82.65 mmol) and titanium tetrachloride (1 M in toluene, 41.33 mL, 41.33 mmol) in 50 mL of dry 1,2-dimethoxyethane to 0° C. under N2. Add 1-(6-chloropyridin-3-yl)ethanone oxime (3.52 g, 20.66 mmol) to the solution dropwise. Stir the mixture overnight at RT. Quench the reaction with 200 mL of water. Basify the mixture with ammonium hydroxide. Subsequently, extract the crude product into toluene and ethyl acetate. Separate the layers and dry the organic layer over sodium sulfate. Concentrate in vacuo to give the crude product (1.24 g, 38%). 1H NMR (400 MHz, CDCl3) δ 3.53 (s, 3H), 5.23 (s, 2H), 7.39 (d, J=4.0 Hz, 1H), 7.96 (d, J=1.6 Hz, 1H).

후처리

  1. customQuench
  2. customthe reaction with 200 mL of water
  3. extractionSubsequently, extract the crude product into toluene and ethyl acetate
  4. customSeparate the layers
  5. dry with materialdry the organic layer over sodium sulfate
  6. concentrationConcentrate in vacuo

출처 및 근거

ORD 기록
ord-14f347a129674ea6a8d76699682436b9
출처 데이터셋
uspto-grants-2012_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08114872B2

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