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Ammonium Hydroxide → 4-(Pyridin-3-yloxy)butan-1-amine

HRID 1168921
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HRID 1168921 반응식
Cl[CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1.[OH-].[NH4+:14]>CO>[N:9]1[CH:10]=[CH:11][CH:12]=[C:7]([O:6][CH2:5][CH2:4][CH2:3][CH2:2][NH2:14])[CH:8]=1
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참가 물질

4

반응물 2

HCID 14923Ammonium HydroxideHCID 229897004-Chloro-1-(3-pyridyloxy)butane

생성물 1

HCID 121122194-(Pyridin-3-yloxy)butan-1-amine수율 74.2%

시약·촉매·용매 1

HCID 887Methanol용매

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온도
100 °C

실험 절차

The 4-chloro-1-(3-pyridyloxy)butane (2.00 g, 10.8 mmol) was dissolved in methanol (25 mL) and added to concentrated ammonium hydroxide solution (29.7%, 14.8 M, 50 mL) in a heavy-walled glass pressure-tube apparatus. The tube was sealed and the mixture was stirred and heated at 100° C. (oil bath temperature) for 6 h. After cooling, the mixture was concentrated by rotary evaporation. Saturated NaCl solution (10 mL) was added to the residue, and the solution (pH 6) was extracted with ether (3×25 mL) to remove impurities. The aqueous layer was basified to pH 10 with 10% NaOH solution, and the mixture was extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (Na2SO4), filtered, and concentrated by rotary evaporation to a residue that was dried briefly under high vacuum to give 1.25 g (74.2%) of an oil.

후처리

  1. customThe tube was sealed
  2. temperatureAfter cooling
  3. concentrationthe mixture was concentrated by rotary evaporation
  4. additionSaturated NaCl solution (10 mL) was added to the residue
  5. extractionthe solution (pH 6) was extracted with ether (3×25 mL)
  6. customto remove impurities
  7. extractionthe mixture was extracted with chloroform (4×25 mL)
  8. dry with materialThe combined chloroform extracts were dried (Na2SO4)
  9. filtrationfiltered
  10. concentrationconcentrated by rotary evaporation to a residue that
  11. customwas dried briefly under high vacuum

출처 및 근거

ORD 기록
ord-ab12d55c719a4b06864f726503b320f9
출처 데이터셋
uspto-grants-2003_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06627648B1

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