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1-[(3-Buten-1-yl)diphenylsilyl]-3-methyl-1-butanone → 1-[(3-Buten-1-yl)diphenylsilyl]-3-methyl-1-butanol

HRID 962822
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 962822
[CH2:1]([Si:5]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[C:6](=[O:11])[CH2:7][CH:8]([CH3:10])[CH3:9])[CH2:2][CH:3]=[CH2:4].[H-].[Al+3].[Li+].[H-].[H-].[H-]>C(OCC)C>[CH2:1]([Si:5]([C:12]1[CH:13]=[CH:14][CH:15]=[CH:16][CH:17]=1)([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)[CH:6]([OH:11])[CH2:7][CH:8]([CH3:10])[CH3:9])[CH2:2][CH:3]=[CH2:4]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 153498501-[(3-Buten-1-yl)diphenylsilyl]-3-methyl-1-butanoneHCID 21226445Aluminium lithium hydride

Produkt 1

HCID 220158361-[(3-Buten-1-yl)diphenylsilyl]-3-methyl-1-butanolAusbeute 69,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 3283Diethyl EtherLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of 33 (3.0 g, 9.3 mmol) in ethyl ether (100 mL) at 0° C. was added lithium aluminum hydride (1.0M in ethyl ether, 47 mmol). After stirring for 15 min at 0° C. under argon, the reaction mixture was diluted with ethyl ether (300 mL) and quenched with saturated aqueous Na2 SO4 until evolution of hydrogen had ceased. The mixture was dried with solid Na2SO4 and filtered, and the residue was extracted with ether (50 mL). The organic extracts were combined and concentrated in vacuo. Flash chromatography over silica gel (1/9 EtOAc:hexane) gave pure 34 as a colorless oil (2.1 g, 69%): R.function. =0.60 (1/9 EtOAc:hexane); 1H NMR (300 MHz, CDCl3) δ6 7.57 (m, 4H), 7.37 (m, 6H), 5.87 (m, 1H), 4.97 (dd, J=17.1, 1.7 Hz, 1H), 4.88 (dd, J=10 2, 1.7 Hz, 1H), 4.08 (d, J=12.1 Hz, 1H), 2.12 (m, 2H), 1.85 (m, 1H), 1.58 (m, 1H), 1.26 (m, 4H), 0.88 (d, J=6.2 Hz, 6H); 13C NMR (75 MHz, CDCl3) δ141.4, 135.7, 133.8, 129.8, 128.2, 113.3, 61.5, 42.4, 27.5, 24.2, 23.7, 20.7, 9.8; IR (neat) 15 3565 (m), 3452 (m, br), 3069 (m), 3050 (m), 2955 (s), 2910 (s), 2869 (m), 1965 (w), 1894 (w), 1832 (w), 1642 (m), 1469 (m), 1434 (s), 1369 (w), 1116 (s), 1001 m), 916 (m), 743 (s), 705 (s) cm-1 ; MS (FAB) m/e (rel. intensity) 323 (MH+ -2, 5), 269 (21), 238 (11), 198 (57), 183 (100), 181 (10), 177 (23), 161 (14), 159 (56), 123 (15), 99 (12); HRMS (FAB) caled for C21H27 0Si: 323.1831 (MH+ -2), found: 323.1824. Anal. Calcd for C21H28SiO: C, 77.72; H, 8.70. Found: C, 77.60; H, 8.67.

Aufarbeitung

  1. customquenched with saturated aqueous Na2 SO4 until evolution of hydrogen
  2. dry with materialThe mixture was dried with solid Na2SO4
  3. filtrationfiltered
  4. extractionthe residue was extracted with ether (50 mL)
  5. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-34267141c8224f508cb19e5e115f08e5
Quelldatensatz
uspto-grants-1998_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05760019

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