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

HRID 1162017
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HRID 1162017 반응식
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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 534071701-Benzyl-3-(trifluoromethyl)piperazine2회

생성물 1

HCID 185197252-(Trifluoromethyl)piperazine

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-b2e7360a89ff45cf960dfb173fcfe8ee
출처 데이터셋
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07820675B2

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