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Benzyl 4-((dimethylphosphinoyl)methyl)piperazine-1-carboxylate → 1-[(Dimethylphosphoryl)methyl]piperazine

HRID 877099
ノート
印刷プレビュー

反応式

HRID 877099 の反応式
[CH3:1][P:2]([CH2:5][N:6]1[CH2:11][CH2:10][N:9](C(OCC2C=CC=CC=2)=O)[CH2:8][CH2:7]1)([CH3:4])=[O:3]>[Pd].CO>[CH3:4][P:2]([CH2:5][N:6]1[CH2:7][CH2:8][NH:9][CH2:10][CH2:11]1)([CH3:1])=[O:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

HCID 67504698Benzyl 4-((dimethylphosphinoyl)methyl)piperazine-1-carboxylate

生成物 1

HCID 203769071-[(Dimethylphosphoryl)methyl]piperazine

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

To a flask was charged with benzyl 4-((dimethylphosphinoyl)methyl)piperazine-1-carboxylate (200 mg) and 10% palladium on carbon in methanol (20 mL). The mixture was stirred at room temperature under H2 atmosphere. The mixture was filtered through Celite and all solvents were removed under reduced pressure to give a white crystalline solid, which was used without further purification. LCMS ESI(+) m/z: 177 (M+1).

後処理

  1. filtrationThe mixture was filtered through Celite
  2. customall solvents were removed under reduced pressure
  3. customto give a white crystalline solid, which
  4. customwas used without further purification

出典と根拠

ORDレコード
ord-3433a2443b704798bda5efe04195b433
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987284B2

反応ノート

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