Ethyl Acetate → 3-[3-(4,5-Diphenyloxazol-2-yl)-3-hydroxy-2-(2-hydroxyethyl)propyl]-1-(t-butyldiphenylsilyloxy)benzene

HRID 380088Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 380088
[C:1]1([C:7]2[N:8]=[CH:9][O:10][C:11]=2[C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.C([Li])CCC.[Si:23]([O:40][C:41]1[CH:42]=[C:43]([CH:51]=[CH:52][CH:53]=1)[CH2:44][CH:45]1[CH2:49][CH2:48][O:47][C:46]1=[O:50])([C:36]([CH3:39])([CH3:38])[CH3:37])([C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1.C(OCC)(=O)C>C1COCC1.O>[C:1]1([C:7]2[N:8]=[C:9]([CH:46]([OH:50])[CH:45]([CH2:49][CH2:48][OH:47])[CH2:44][C:43]3[CH:42]=[C:41]([O:40][Si:23]([C:36]([CH3:38])([CH3:39])[CH3:37])([C:24]4[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=4)[C:30]4[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=4)[CH:53]=[CH:52][CH:51]=3)[O:10][C:11]=2[C:12]2[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Komponenten

7

Edukt 4

HCID 8857Ethyl AcetateHCID 6134984,5-DiphenyloxazoleHCID 183672193-(3-t-Butyldiphenylsilyloxybenzyl)-2-oxotetrahydrofuranHCID 178418339Butyllithium

Produkt 1

HCID 183674053-[3-(4,5-Diphenyloxazol-2-yl)-3-hydroxy-2-(2-hydroxyethyl)propyl]-1-(t-butyldiphenylsilyloxy)benzeneAusbeute 85,8 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To a solution of 4,5-diphenyloxazole (5.3 g) in THF (50 ml) at −78° C. under N2 was added n-butyllithium (1.6 M in hexane, 9.2 ml). After 30 minutes, a solution of 3-(3-t-butyldiphenylsilyloxybenzyl)-2-oxotetrahydrofuran (3.3 g) in THF (30 ml) was added thereto and stirred for 1 hour at the same temperature. The reaction mixture was poured into the mixture of ethyl acetate and water. The organic layer was washed with 1N-HCl solution, sat. NaHCO3 and brine, dried over MgSO4, and evaporated in vacuo. The oily residue was dissolved in THF (100 ml) and LiAlH4 was added to the solution at 0° C. After being stirred for 2 hours, the mixture was poured into a mixture of ethyl acetate and 1N-HCl solution. The organic layer was washed with sat. NaHCO3 and brine, dried over MgSO4, and evaporated in vacuo. The residue was purified by chromatography on silica gel to afford 3-[3-(4,5-diphenyloxazol-2-yl)-3-hydroxy-2-(2-hydroxyethyl)propyl]-1-(t-butyldiphenylsilyloxy)benzene (4.3 g).

Aufarbeitung

  1. washThe organic layer was washed with 1N-HCl solution, sat. NaHCO3 and brine
  2. dry with materialdried over MgSO4
  3. customevaporated in vacuo
  4. dissolutionThe oily residue was dissolved in THF (100 ml)
  5. additionLiAlH4 was added to the solution at 0° C
  6. stirringAfter being stirred for 2 hours
  7. additionthe mixture was poured into a mixture of ethyl acetate and 1N-HCl solution
  8. washThe organic layer was washed with sat. NaHCO3 and brine
  9. dry with materialdried over MgSO4
  10. customevaporated in vacuo
  11. customThe residue was purified by chromatography on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-18ddec2c802644e990bee1867d3ed471
Quelldatensatz
uspto-grants-2001_10
Patentnummer
US06300344B1

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