Acetic Acid → N-Cyclohexyl-1,2-ethanediamine

HRID 1776248

反応式

HRID 1776248 の反応式
[C:1]1(=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[CH2:8]([NH2:11])[CH2:9][NH2:10].C(O)(=O)C.C([BH3-])#N.[Na+]>CO>[CH:1]1([NH:10][CH2:9][CH2:8][NH2:11])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1

参加物

6

実験手順

To a solution of cyclohexanone (6.260 g, 63.8 mmol), ethylenediamine (42.640 mL, 637.8 mmol), acetic acid (36.515 mL, 637.8 mmol), and 4 {acute over (Å)} molecular sieves (25 g) in anhydrous methanol (250 mL) was added sodium cyanoborohydride (8.017 g, 127.6 mmol). The mixture was stirred for 48 hrs, filtered to remove the solids, and concentrated in vacuo. The residue was dissolved in 3 N aqueous sodium hydroxide (150 mL) and extracted with methylene chloride (3×300 mL). The combined organic layers were washed with basic saturated aqueous sodium chloride, dried (anhydrous sodium sulfate), filtered, and concentrated to give the crude product. The material was vacuum distilled to give the desired product as a clear liquid (4.1 g, 45%). 1H NMR (300 MHz, CDCl3) δ 2.80-2.76 (td, 2H, J=0.9, 6.0 Hz), 2.68-2.64 (td, 2H, J=0.9, 6.0 Hz), 2.43-2.34 (m, 1H), 1.89-1.83 (m, 2H), 1.74-1.70 (m, 2H), 1.62-1.57 (m, 1H), 1.32-0.98 (m, 8H).

後処理

  1. filtrationfiltered
  2. customto remove the solids
  3. concentrationconcentrated in vacuo
  4. dissolutionThe residue was dissolved in 3 N aqueous sodium hydroxide (150 mL)
  5. extractionextracted with methylene chloride (3×300 mL)
  6. washThe combined organic layers were washed with basic saturated aqueous sodium chloride
  7. dry with materialdried (anhydrous sodium sulfate)
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customto give the crude product
  11. distillationdistilled

出典と根拠

ORDレコード
ord-8462f7971b6845c0bee83a274715b6e9
出典データセット
uspto-grants-2016_02
特許番号
US09265772B2

関連ノート

読み込み中…