Cyclohexanone → 1-Cyclohexylpyrrolidine

HRID 1167037Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1167037
[NH:1]1[CH2:5][CH2:4][CH2:3][CH2:2]1.[C:6]1(=O)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1.S([O-])([O-])(=O)=O.[Mg+2]>CCCCCC>[CH:6]1([N:1]2[CH2:5][CH2:4][CH2:3][CH2:2]2)[CH2:11][CH2:10][CH2:9][CH2:8][CH2:7]1

Komponenten

5

Edukt 3

HCID 7967CyclohexanoneHCID 24083Sulfuric acid magnesium salt (1:1)HCID 31268Pyrrolidine

Produkt 1

HCID 1390641-Cyclohexylpyrrolidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8058HexaneLösungsmittel

Versuchsvorschrift

The structure-directing agent (SDA) is synthesized using the reaction sequence described in the scheme below. A three neck 3000-ml flask is charged with 100 gm (1.4 mole) of pyrrolidine, 50 gm of cyclohexanone (0.51 mole) and 1000 ml anhydrous hexane. To the resulting solution, 122 gm (1.022 mole) of anhydrous magnesium sulfate is added and the mixture is mechanically stirred and heated at reflux (the reaction is monitored by NMR analysis) for 96 hrs. The reaction mixture is filtered through a fritted glass funnel. The filtrate is concentrated under reduced pressure on a rotary evaporator to give 75 gm of a clear (yellow-tinted) oily substance. 1H-NMR and 13C-NMR spectra are acceptable for the desired product 1-(1-pyrrolidino)cyclohexene. Saturation of 1-(1-pyrrolidino)cyclohexene, to give N-cyclohexylpyrrolidine, is accomplished in quantitative yield by hydrogenation in ethanol at a 55 psi pressure of hydrogen gas in the presence of 10% Pd on activated carbon.

Aufarbeitung

  1. customThe structure-directing agent (SDA) is synthesized
  2. temperatureheated
  3. temperatureat reflux (the reaction
  4. customfor 96 hrs
  5. filtrationThe reaction mixture is filtered through a fritted glass funnel
  6. concentrationThe filtrate is concentrated under reduced pressure on a rotary evaporator
  7. customto give 75 gm of a clear (yellow-tinted) oily substance

Quellen und Nachweise

ORD-Eintrag
ord-58b0165414764fd1bf7e6d281b469dc9
Quelldatensatz
uspto-grants-2003_09
Patentnummer
US06616911B2

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