2-Iodohexane → 4-Hydroxy-1-Hexylpiperidine

HRID 1107565

反応式

HRID 1107565 の反応式
[OH:1][CH:2]1[CH2:7][CH2:6][NH:5][CH2:4][CH2:3]1.I[CH:9]([CH2:11][CH2:12][CH2:13][CH3:14])[CH3:10]>CC(CC)=O>[OH:1][CH:2]1[CH2:7][CH2:6][N:5]([CH2:10][CH2:9][CH2:11][CH2:12][CH2:13][CH3:14])[CH2:4][CH2:3]1

参加物

4

実験手順

4-Hydroxypiperidine (2.02 g, 20 mmol) was dissolved in 100 mL of methyl ethylketone. To this stirred mixture was added 2-iodohexane (1.5 mL, 10 mmol) and the resulting solution was heated at reflux for 1.5 hours. The mixture was allowed to cool and was then washed with saturated aqueous sodium bicarbonate (3×75 mL). The organic layer was dried over magnesium sulfate, filtered, and evaporated, and the residue was dried overnight under house vacuum to yield 1.184 g (64%) of the title compound which was used without further purification. 1H NMR consistent with desired product. MS(FD) 186(M+).

後処理

  1. temperaturethe resulting solution was heated
  2. temperatureat reflux for 1.5 hours
  3. temperatureto cool
  4. washwas then washed with saturated aqueous sodium bicarbonate (3×75 mL)
  5. dry with materialThe organic layer was dried over magnesium sulfate
  6. filtrationfiltered
  7. customevaporated
  8. customthe residue was dried overnight under house vacuum

出典と根拠

ORDレコード
ord-e3f26c66634643b08fe45bb101c390a3
出典データセット
uspto-grants-2000_05
特許番号
US06060488

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