1-Diphenylmethylamino-2-phenylethylphosphonous acid → 1-Amino-2-phenylethylphosponous acid

HRID 1376425ノート

反応式

HRID 1376425 の反応式
C1(C([NH:14][CH:15]([P:23]([OH:25])[OH:24])[CH2:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)C2C=CC=CC=2)C=CC=CC=1>Br>[NH2:14][CH:15]([P:23]([OH:25])[OH:24])[CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

参加物

3

反応物 1

HCID 229165271-Diphenylmethylamino-2-phenylethylphosphonous acid

生成物 1

HCID 229165291-Amino-2-phenylethylphosponous acid

試薬・触媒・溶媒 1

HCID 260Hydrogen Bromide溶媒

実験手順

9.9 g (0.028 mol) of 1-diphenylmethylamino-2-phenylethylphosphonous acid are heated, at 100°-105° C. for 2 h, in 50 ml of 40% hydrobromic acid. The reaction solution is then evaporated to dryness i.V. and the residue is taken up in 50 ml of water. The aqueous solution is washed several times with diethyl ether and evaporated to dryness. The residue is dissolved in 60 ml of ethanol and propylene oxide is added to the solution until the product precipitates out. After the mixture has been left to stand overnight, the precipitate is filtered off with suction, washed with ethanol/diethyl ether and dried.

後処理

  1. customThe reaction solution is then evaporated to dryness i.V
  2. washThe aqueous solution is washed several times with diethyl ether
  3. customevaporated to dryness
  4. dissolutionThe residue is dissolved in 60 ml of ethanol
  5. additionpropylene oxide is added to the solution until the product
  6. customprecipitates out
  7. waitAfter the mixture has been left
  8. filtrationthe precipitate is filtered off with suction
  9. washwashed with ethanol/diethyl ether
  10. customdried

出典と根拠

ORDレコード
ord-9aa50f4c9c224ff5aefb63bcf3db20c3
出典データセット
uspto-grants-1997_09
特許番号
US05663139

反応ノート

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