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Trifluoroacetic acid → [(2S)-2-Methyl-1-piperazinyl]phenylmethanone

HRID 1689959
ノート
印刷プレビュー

反応式

HRID 1689959 の反応式
[C:1]([N:9]1[CH2:14][CH2:13][N:12](C(OC(C)(C)C)=O)[CH2:11][C@@H:10]1[CH3:22])(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.FC(F)(F)C(O)=O>ClCCl>[CH3:22][C@H:10]1[CH2:11][NH:12][CH2:13][CH2:14][N:9]1[C:1]([C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1)=[O:8]
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 2

HCID 6422Trifluoroacetic acidHCID 57581556HCID 57581556、化合物

生成物 1

HCID 57581475[(2S)-2-Methyl-1-piperazinyl]phenylmethanone

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

(S)-tert-butyl 4-benzoyl-3-methylpiperazine-1-carboxylate (8.16 g, 26.8 mmol) was dissolved in dichloromethane (200 mL). Trifluoroacetic acid (20.7 ml) was added and the reaction was stirred at rt for 1.5 hours. The reaction was quenched into saturated K2CO3 (30 mL) and neutralized by the portion-wise addition of solid NaHCO3. The layers were separated and extracted twice with dichloromethane. The combined organics were dried (MgSO4) and evaporated to give a yellow oil. MS (M+H)+=205.3.

後処理

このページの内容参加物実験手順後処理出典と根拠反応ノート
  1. customThe reaction was quenched into saturated K2CO3 (30 mL)
  2. additionneutralized by the portion-wise addition of solid NaHCO3
  3. customThe layers were separated
  4. extractionextracted twice with dichloromethane
  5. dry with materialThe combined organics were dried (MgSO4)
  6. customevaporated
  7. customto give a yellow oil

出典と根拠

ORDレコード
ord-cb30c2f8c58b427298c22302d42b8756
出典データセット
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08153633B2

反応ノート

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