Glycine → Glycine, N-cyclohexyl-

HRID 849436

反応式

HRID 849436 の反応式
[NH2:1][CH2:2][C:3]([OH:5])=[O:4].[C:6]1(=O)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.[H][H]>[Pd].C(O)(=O)C>[CH:6]1([NH:1][CH2:2][C:3]([OH:5])=[O:4])[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1

参加物

6

実験手順

Similar equipment and procedure as described in Example 1 were employed. 75.5 grams glycine (1.01 moles, Aldrich, 99+%), 118.4 grams cyclohexanone (1.21 moles, Aldrich 99.8%), 300 ml glacial acetic acid and 11.2 grams of Pd (5%)/C were used. The reaction was carried out in a 600 ml Parr reactor under 1000 psig (7000 kPa) hydrogen pressure at 75° C. No noticeable hydrogen uptake was noticed after 1.5 days, and the reaction was carried out for 4.5 days. The reactor was opened after cooling to room temperature. The solid catalyst was filtered by suction. The filtrate was evaporated to remove the acetic acid and the excess cyclohexanone. A viscous crude product (brown) remained which started to crystallize upon cooling to room temperature. The crude product was stirred into excess ether whereby a white solid precipitated out. The solid was filtered, washed with ether and dried. The solid was redissolved in a very small amount of acetic acid and recrystallized by adding an appropriate amount of ether. 144.5 grams of white crystals were recovered (91% yield based on glycine). Elemental analysis:calculated: C:61.12; H:9.62; N:8.91; 0:20.36; found:C:60.96; H:9.75; N:8.88; 0:20.41.

後処理

  1. filtrationThe solid catalyst was filtered by suction
  2. customThe filtrate was evaporated
  3. customto remove the acetic acid
  4. customto crystallize
  5. temperatureupon cooling to room temperature
  6. customprecipitated out
  7. filtrationThe solid was filtered
  8. washwashed with ether
  9. customdried
  10. dissolutionThe solid was redissolved in a very small amount of acetic acid
  11. customrecrystallized
  12. additionby adding an appropriate amount of ether
  13. custom144.5 grams of white crystals were recovered (91% yield based on glycine)

出典と根拠

ORDレコード
ord-812d32df2c1748b7be5316f9574ca740
出典データセット
uspto-grants-2000_01
特許番号
US06013239

関連ノート

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