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

HRID 1162017
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1162017
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
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 1

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

Produkt 1

HCID 185197252-(Trifluoromethyl)piperazine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 23938PalladiumKatalysatorHCID 176Acetic AcidLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-b2e7360a89ff45cf960dfb173fcfe8ee
Quelldatensatz
uspto-grants-2010_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07820675B2

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