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Imidazole → [t-Butyl(dimethyl)silyloxymethyl]-2-piperidone

HRID 467234
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 467234
[Si:1](Cl)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].OC[CH:11]1[CH2:16][NH:15][C:14](=[O:17])[CH2:13][CH2:12]1.N1C=CN=C1.CN([CH:26]=[O:27])C>>[Si:1]([O:27][CH2:26][N:15]1[CH2:16][CH2:11][CH2:12][CH2:13][C:14]1=[O:17])([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 4

HCID 795ImidazoleHCID 6228DimethylformamideHCID 28928tert-Butyldimethylsilyl chlorideHCID 153860795-(Hydroxymethyl)piperidin-2-one

Produkt 1

HCID 21760387[t-Butyl(dimethyl)silyloxymethyl]-2-piperidone

Reaktionsbedingungen

Temperatur
22 °C

Versuchsvorschrift

To a solution of 5.8 g tert-butyl(dimethyl)silyl chloride and 5.0 g of 5-hydroxymethyl-2-piperidone in 150 ml of anhydrous DMF was added 5.3 g of imidazole. After stirring for 36 hours at 22° C., the mixture was evaporated under vacuum to remove most of the DMF. Following the addition of water, the residue was extracted with three portions of ethyl acetate. The combined organic extracts were washed with water, 0.5N HCl, water and brine, dried over magnesium sulfate and evaporated. The resulting oil was chromatographed over silica gel eluting with 5% methanol in chloroform to give 4.7 g of the title compound as an oil: MS m/z 244 (M+), 186 [M+ -58(t-butyl)]; 300-MHz 1H NMR (CDCl3) δ0.05 (s, 6 H), 0.85 (s, 9 H), 1.42-1.57 (m, 1 H), 1.77-1.88 (m, 1 H), 1.89-2.03 (m, 1 H), 2.25- 2.45 (m, 2 H), 3.03 (t, J=9 Hz, 1 H), 3.30-3.41 (m, 1 H), 3.45-3.59 (m, 2 H), 5.95 (s, 1 H).

Aufarbeitung

  1. customthe mixture was evaporated under vacuum
  2. customto remove most of the DMF
  3. additionthe addition of water
  4. extractionthe residue was extracted with three portions of ethyl acetate
  5. washThe combined organic extracts were washed with water, 0.5N HCl, water and brine
  6. dry with materialdried over magnesium sulfate
  7. customevaporated
  8. customThe resulting oil was chromatographed over silica gel eluting with 5% methanol in chloroform

Quellen und Nachweise

ORD-Eintrag
ord-09999afcdf5e4439943c9d215c2b8fc0
Quelldatensatz
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05159079

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