Dimethylformamide → 4-(Diphenylmethyl)-1-piperazineethanol

HRID 746241

Reaktionsgleichung

Reaktionsgleichung von HRID 746241
[N:1]1([CH2:7][CH2:8][OH:9])[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.C(=O)([O-])[O-].[K+].[K+].CN(C)C=O.[CH:21](Br)([C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>O>[CH:21]([N:4]1[CH2:5][CH2:6][N:1]([CH2:7][CH2:8][OH:9])[CH2:2][CH2:3]1)([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1)[C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1

Komponenten

6

Edukt 4

HCID 6228DimethylformamideHCID 76771-(2-Hydroxyethyl)piperazineHCID 11430Potassium CarbonateHCID 236603Bromodiphenylmethane

Produkt 1

HCID 47425734-(Diphenylmethyl)-1-piperazineethanolAusbeute 84,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 962WaterLösungsmittel

Versuchsvorschrift

To a mixture of 1-piperazineethanol (11.4 g), potassium carbonate powder (24.3 g) and N,N-dimethylformamide (100 ml) was added dropwise benzhydryl bromide (21.7 g). The mixture was stirred at room temperature for 2 hours, then diluted with water and extracted with ethyl ether. The ethyl ether layer was washed with saturated aquus sodium chloride and dried over sodium sulfate. The solvent was then distilled off and the residue was purified by silica gel chromatography [eluent: hexane-ethyl acetate (2:1)] to give 21.9 g (84.2%) of 4-benzhydryl-1-piperazineethanol as an oil.

Aufarbeitung

  1. extractionextracted with ethyl ether
  2. washThe ethyl ether layer was washed with saturated aquus sodium chloride
  3. dry with materialdried over sodium sulfate
  4. distillationThe solvent was then distilled off
  5. customthe residue was purified by silica gel chromatography [eluent: hexane-ethyl acetate (2:1)]

Quellen und Nachweise

ORD-Eintrag
ord-a7f89949a20b48bfbffc559b3f3b5a68
Quelldatensatz
uspto-grants-1986_07
Patentnummer
US04603135

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