2,2-Dimethyl-1-[4-(4-nitro-phenyl)-piperazin-1-yl]-propan-1-one → 1-(2,2-Dimethyl-propyl)-4-(4-nitro-phenyl)-piperazine

HRID 37845

Reaktionsgleichung

Reaktionsgleichung von HRID 37845
[CH3:1][C:2]([CH3:21])([CH3:20])[C:3]([N:5]1[CH2:10][CH2:9][N:8]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)[CH2:7][CH2:6]1)=O>C1COCC1>[CH3:1][C:2]([CH3:21])([CH3:20])[CH2:3][N:5]1[CH2:6][CH2:7][N:8]([C:11]2[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=2)[CH2:9][CH2:10]1

Komponenten

3

Versuchsvorschrift

A solution of 2,2-dimethyl-1-[4(4-nitro-phenyl)-piperazin-1-yl]-propan-1-one (8.0 g, 27.5 mmol) in THF (100 mL) was added dropwise to a solution of borane-dimethylsulfide complex (16 mL, 166 mmol) in THF (100 mL) over 30 minutes and stirred for 3 h at room temperature. The mixture was quenched with saturated ammonium chloride solution (200 mL) and concentrated to remove organic solvents under reduced pressure (<45° C.). The aqueous layer was extracted with ethyl acetate (3×100 mL) then the combined extracts were washed with water (100 mL) and brine (100 mL), dried over sodium sulfate and concentrated to dryness to afford 1-(2,2-dimethyl-propyl)-4-(4-nitro-phenyl)-piperazine (6 g, 79%) as a yellow solid.

Aufarbeitung

  1. customThe mixture was quenched with saturated ammonium chloride solution (200 mL)
  2. concentrationconcentrated
  3. customto remove organic solvents under reduced pressure (<45° C.)
  4. extractionThe aqueous layer was extracted with ethyl acetate (3×100 mL)
  5. washthe combined extracts were washed with water (100 mL) and brine (100 mL)
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated to dryness

Quellen und Nachweise

ORD-Eintrag
ord-18f7e4e37b414933985efe06210a5699
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08524705B2

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