Butanal → 3-(2-Propenyl)-4-t-butyldimethylsilyloxy-2-(1-hydroxybutyl)cyclopentanone

HRID 35488

Reaktionsgleichung

Reaktionsgleichung von HRID 35488
C(P(CCCC)CCCC)CCC.[CH2:14]([Li])[CH:15]=[CH2:16].[Si:18]([O:25][CH:26]1[CH2:30][C:29](=[O:31])[CH:28]=[CH:27]1)([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19].[CH:32](=[O:36])[CH2:33][CH2:34][CH3:35].[Cl-].[NH4+]>CCOCC.C(OCC)(=O)C.C1C=CC=CC=1>[CH2:14]([CH:27]1[CH:26]([O:25][Si:18]([C:21]([CH3:24])([CH3:23])[CH3:22])([CH3:20])[CH3:19])[CH2:30][C:29](=[O:31])[CH:28]1[CH:32]([OH:36])[CH2:33][CH2:34][CH3:35])[CH:15]=[CH2:16]

Komponenten

9

Edukt 5

HCID 261ButanalHCID 13831TributylphosphineHCID 25517Ammonium ChlorideHCID 41316994-((tert-Butyl(dimethyl)silyl)oxy)cyclopent-2-en-1-oneHCID 178506856HCID 178506856, Verbindung

Produkt 1

HCID 212962343-(2-Propenyl)-4-t-butyldimethylsilyloxy-2-(1-hydroxybutyl)cyclopentanoneAusbeute 44 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 241BenzeneLösungsmittelHCID 3283Diethyl EtherLösungsmittel3×HCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

266 mg (2.2 mmoles) of 2-bromopropene was dissolved in 5 ml of dry ether, and the solution was cooled to -95° C. Then, 3.0 ml (4.8 mmoles) of t-butyllithium (as 1.60M pentane solution) was added, and the mixture was stirred at -78° C. for 2 hours to form a 2-propenyllithium solution. 300 mg (2.05 mmoles) of cuprous iodide was taken into a reaction vessel. The reaction vessel was purged with argon, and 30 ml of dry ether and 1.02 ml (4.1 mmoles) of tributyl phosphine were added. The mixture was stirred for 10 minutes. The mixture was added to the 2-propenyllithium solution prepared above, and the mixture was stirred for 5 minutes. A solution of 425 mg (2.0 mmoles) of 4-t-butyldimethylsilyloxy-2-cyclopentenone in 5 ml of dry ether was added. The mixture was stirred at -78° C. for 10 minutes and -40° C. for 20 minutes. A solution of 148 mg (2.05 mmoles) of butanal in 5 ml of dry ether was added, and the mixture was stirred at -40° C. for 1 hour. 50 ml of a saturated aqueous solution of ammonium chloride was added, and the mixture was extracted with ether. The etheric layers were combined, dried over anhydrous magnesium sulfate, filtered, concentrated and then subjected to silica gel column chromatography (silica gel 50 g; eluent, benzene:ethyl acetate=10:1→3:1 to give 287 mg (yield 44%) of 3-(2-propenyl)-4-t-butyldimethylsilyloxy-2-(1-hydroxybutyl)cyclopentanone. The resulting compound had the following spectral data.

Aufarbeitung

  1. additionwere added
  2. customprepared above, and the mixture
  3. stirringwas stirred for 5 minutes
  4. stirringThe mixture was stirred at -78° C. for 10 minutes and -40° C. for 20 minutes
  5. stirringthe mixture was stirred at -40° C. for 1 hour
  6. extractionthe mixture was extracted with ether
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-9557bcdf92b34f94adc10514da842f42
Quelldatensatz
uspto-grants-1988_08
Patentnummer
US04766147

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