Potassium Carbonate → t-Butyl 4-carboethoxypropyl-1-piperazinecaboxylate

HRID 429499

Reaktionsgleichung

Reaktionsgleichung von HRID 429499
[N:1]1([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.Cl[CH2:15][CH2:16][CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19].C(=O)([O-])[O-].[K+].[K+].C(OCC)(=O)C.CCCCCC>CN(C)C=O.C(=O)(O)[O-].[Na+]>[C:18]([CH2:17][CH2:16][CH2:15][N:4]1[CH2:5][CH2:6][N:1]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:2][CH2:3]1)([O:20][CH2:21][CH3:22])=[O:19]

Komponenten

7

Versuchsvorschrift

Combine t-butyl 1-piperazinecarboxylate (10.7 g, 57.5 mmol), ethyl 4-chlorobutyrate (10.4 mL), and potassium carbonate (8 g) in dimethylformamide (60 mL). Heat at reflux. After 4.5, hours, cool the reaction, dilute with an aqueous solution of sodium bicarbonate, and extract twice with diethyl ether (200 mL). Combine the organic layers and extract with a 1 M aqueous solution of hydrochloric acid. Adjust the pH of the aqueous layer to basic using sodium bicarbonate and then extract twice with diethyl ether. Dry the combined organic layers over MgSO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting sequentially with 10% ethyl acetate/hexane, 20% ethyl acetate/hexane, 25% ethyl acetate/hexane to give t-butyl 4-carboethoxypropyl-1-piperazinecaboxylate. Rf=0.5 (silica gel, ethyl acetate).

Aufarbeitung

  1. temperatureHeat
  2. temperatureat reflux
  3. temperatureAfter 4.5, hours, cool
  4. customthe reaction
  5. extractionextract twice with diethyl ether (200 mL)
  6. extractionCombine the organic layers and extract with a 1 M aqueous solution of hydrochloric acid
  7. extractionextract twice with diethyl ether
  8. dry with materialDry the combined organic layers over MgSO4
  9. filtrationfilter
  10. customevaporate in vacuo
  11. customto give a residue

Quellen und Nachweise

ORD-Eintrag
ord-54eb7d5e4ac64844ad5fd2ad77131847
Quelldatensatz
uspto-grants-2001_11
Patentnummer
US06316445B1

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