Ethyl chloroformate → Nalphaethoxycarbonyl-DL-methionine amide

HRID 1602758ノート

反応式

HRID 1602758 の反応式
[CH2:1]([O:3][C:4](Cl)=[O:5])[CH3:2].[NH2:7][CH:8]([C:13]([NH2:15])=[O:14])[CH2:9][CH2:10][S:11][CH3:12].[OH-].[Na+]>O>[CH2:1]([O:3][C:4]([NH:7][CH:8]([C:13]([NH2:15])=[O:14])[CH2:9][CH2:10][S:11][CH3:12])=[O:5])[CH3:2]

参加物

5

反応物 3

HCID 10928Ethyl chloroformateHCID 14798Sodium HydroxideHCID 5687422-Amino-4-(methylthio)butanamide

生成物 1

HCID 18329560Nalphaethoxycarbonyl-DL-methionine amide収率 57.4%

試薬・触媒・溶媒 1

HCID 962Water溶媒2 回

反応条件

温度
2.5 °C

実験手順

106 ml (1.10 moles) ethylchloroformate were dripped into a solution of 150 g (1.02 moles) DL-methionine amide in 200 ml water at 5-10° C., during which the pH was maintained at 7-9 by adding sodium hydroxide solution. A thick, finely crystalline precipitate rapidly formed. A suspension which was just able to still be agitated was obtained by the addition of 800 ml water which suspension was agitated 3 hours further at room temperature. Then the colorless crystals were filtered off, washed with water and recrystallized out of 900 ml water. After cooling to 0-5° C., filtering off, washing with water and drying, 129 g (57%) Nα ethoxycarbonyl-DL-methionine amide with a melting point of 110-112° C. were obtained.

後処理

  1. temperaturewas maintained at 7-9
  2. customA thick, finely crystalline precipitate rapidly formed
  3. stirringwas agitated 3 hours further at room temperature
  4. filtrationThen the colorless crystals were filtered off
  5. washwashed with water
  6. customrecrystallized out of 900 ml water
  7. filtrationfiltering off
  8. washwashing with water
  9. customdrying

出典と根拠

ORDレコード
ord-5bf279ec0a2f4040a5f0d7aec96c439e
出典データセット
uspto-grants-1999_11
特許番号
US05985632

反応ノート

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