Methylamine → Methyl(4-(3-pyridyloxy)butyl)amine

HRID 2305701ノート

反応式

HRID 2305701 の反応式
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.[CH3:13][NH2:14]>CO>[CH3:13][NH:14][CH2:2][CH2:3][CH2:4][CH2:5][O:6][C:7]1[CH:8]=[N:9][CH:10]=[CH:11][CH:12]=1

参加物

4

反応条件

温度
100 °C

実験手順

The 4-chloro-1-(3-pyridyloxy)butane (2.00 g, 10.8 mmol) was dissolved in methanol (25 mL) and added to a 40 wt % aqueous solution of methylamine (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 4 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 100% 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 1.47 g (75.5%) of an oil.

後処理

  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

出典と根拠

ORDレコード
ord-6f66983fada8465f851f8fd911db6e01
出典データセット
uspto-grants-2002_08
特許番号
US06441006B2

反応ノート

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