Benzyl chloroformate → 1-Carbobenzyloxyamino-2-methylpropanephosphonous acid

HRID 25986

反応式

HRID 25986 の反応式
[NH2:1][CH:2]([P:6]([OH:8])[OH:7])[CH:3]([CH3:5])[CH3:4].[OH-].[Na+].Cl[C:12]([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13]>O>[C:12]([NH:1][CH:2]([P:6]([OH:8])[OH:7])[CH:3]([CH3:5])[CH3:4])([O:14][CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[O:13]

参加物

5

反応物 3

HCID 10387Benzyl chloroformateHCID 14798Sodium Hydroxide2 回HCID 161274031-Amino-2-methylpropylphosphonous acid

生成物 1

HCID 213258521-Carbobenzyloxyamino-2-methylpropanephosphonous acid

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

27.5 parts of DL-1-amino-2-methylpropanephosphonous acid in 100 parts of water was stirred until solution occurred. The pH of the solution was adjusted to 9.5 with 4N sodium hydroxide and the mixture cooled to 0°. 34 Parts of benzyl chloroformate was added over 1 hour and the mixture stirred for 6 hours maintaining at pH 9.0-9.5 by periodic addition of 4N sodium hydroxide. The mixture was allowed to warm up to room temperature and then washed with ether. The aqueous portion was added slowly to a mixture of 120 parts of water and 80 parts of concentrated hydrochloric acid and 400 parts of ice. The solid which was obtained was dried and recrystallised from ethyl acetate/petroleum ether to give DL-1-carbobenzyloxyamino-2-methylpropanephosphonous acid, melting point 108°-111°.

後処理

  1. temperaturethe mixture cooled to 0°
  2. washwashed with ether
  3. additionThe aqueous portion was added slowly to a mixture of 120 parts of water and 80 parts of concentrated hydrochloric acid and 400 parts of ice
  4. customThe solid which was obtained
  5. customwas dried
  6. customrecrystallised from ethyl acetate/petroleum ether

出典と根拠

ORDレコード
ord-455fa7511e334104a47a191a8969de7c
出典データセット
uspto-grants-1979_04
特許番号
US04147780

関連ノート

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