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HCID 53980652、化合物 → 2-(Pyridin-3-yl)propan-1-amine

HRID 361381
ノート
印刷プレビュー

反応式

HRID 361381 の反応式
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]([CH3:12])[CH2:8][N+:9]([O-])=O)[CH:2]=1>C(O)C.Cl.[Pd]>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]([CH3:12])[CH2:8][NH2:9])[CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 53980652HCID 53980652、化合物

生成物 1

HCID 433168132-(Pyridin-3-yl)propan-1-amine

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 313Hydrochloric Acid溶媒HCID 702Ethanol溶媒

実験手順

To a solution of 2-(3-pyridyl)-1-nitropropane (0.91 g, 5.48 mmol) in 20 mL of ethanol and 0.1 mL of 12N HCl was added 10% Pd/C (1.00 g) under argon. The solution was evacuated and flushed with hydrogen several times, place under an atmosphere of hydrogen and vigorously stirred. After 14 h the mixture was evacuated and flushed with argon several times, filtered through celite and washed with 200 mL of ethanol. The volatiles were removed in vacuo to provide a residue which was partitioned between methylene chloride (100 mL) and NaOH (50 mL, 10%) and the aqueous layer was extracted with methylene chloride (2×100 mL). The combined organic layers were dried over MgSO4, filtered, concentrated in vacuo and the residue was purified by flash column chromatography (20×150 mm column of SiO2, CH2Cl2 /CH2Cl2 saturated with NH3 /MeOH 60:39:1) to give the title compound as an oil:

後処理

  1. customThe solution was evacuated
  2. customflushed with hydrogen several times, place under an atmosphere of hydrogen
  3. customAfter 14 h the mixture was evacuated
  4. customflushed with argon several times
  5. filtrationfiltered through celite
  6. washwashed with 200 mL of ethanol
  7. customThe volatiles were removed in vacuo
  8. customto provide a residue which
  9. customwas partitioned between methylene chloride (100 mL) and NaOH (50 mL, 10%)
  10. extractionthe aqueous layer was extracted with methylene chloride (2×100 mL)
  11. dry with materialThe combined organic layers were dried over MgSO4
  12. filtrationfiltered
  13. concentrationconcentrated in vacuo
  14. customthe residue was purified by flash column chromatography (20×150 mm column of SiO2, CH2Cl2 /CH2Cl2 saturated with NH3 /MeOH 60:39:1)

出典と根拠

ORDレコード
ord-1f6c10c6596a4714aa6a4e5c3df11e7c
出典データセット
uspto-grants-1999_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05866573

反応ノート

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