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1-Benzyl-3-(trifluoromethyl)piperazine → 2-(Trifluoromethyl)piperazine

HRID 1162017
ノート
印刷プレビュー

反応式

HRID 1162017 の反応式
C([N:8]1[CH2:13][CH2:12][NH:11][CH:10]([C:14]([F:17])([F:16])[F:15])[CH2:9]1)C1C=CC=CC=1>C(O)(=O)C.O.[Pd]>[F:15][C:14]([F:17])([F:16])[CH:10]1[CH2:9][NH:8][CH2:13][CH2:12][NH:11]1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 1

HCID 534071701-Benzyl-3-(trifluoromethyl)piperazine2 回

生成物 1

HCID 185197252-(Trifluoromethyl)piperazine

試薬・触媒・溶媒 3

HCID 23938Palladium触媒HCID 176Acetic Acid溶媒HCID 962Water溶媒

実験手順

1-Benzyl-3-(trifluoromethyl)piperazine (0.74 g, 3.0 mmol; Intermediate 44) was dissolved in acetic acid (70 mL) and water (5 mL). Pd, 5% on carbon, (0.074 g) was added and =hydrogenation was performed at 3 bar and 70° C. overnight. The reaction mixture was filtered through Celite and the pad was rinsed with water (5 mL). Solvents were removed in vacuo, toluene (20 mL) added to the residue, followed by re-concentration in vacuo to remove residual water. The desired product sublimated on the evaporator and 0.15 g (32%) was collected as a white powder. 1H NMR (270 MHz, methanol-d4) δ ppm 2.67-2.87 (m, 3H) 2.91-3.05 (m, 2H) 3.12-3.21 (m, 1H). MS (ESI+) m/z 155. *Previously described in Rec. Trav. Chim. Pays-Bas 1995, 114, 97-102.

後処理

  1. customwas performed at 3 bar and 70° C. overnight
  2. filtrationThe reaction mixture was filtered through Celite
  3. washthe pad was rinsed with water (5 mL)
  4. customSolvents were removed in vacuo, toluene (20 mL)
  5. additionadded to the residue
  6. concentrationfollowed by re-concentration in vacuo
  7. customto remove residual water
  8. customThe desired product sublimated on the evaporator and 0.15 g (32%)
  9. customwas collected as a white powder

出典と根拠

ORDレコード
ord-b2e7360a89ff45cf960dfb173fcfe8ee
出典データセット
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07820675B2

反応ノート

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