Reaktion #2314290

ord-d061030504034931b997d04d806f93a4

Reaktionsgleichung

CCCCCC1CCC(C=O)CC1
cyclohexanal
CCCCCC1CCC(C=O)CC1
4-Pentylcyclohexanal
[Br-].c1ccc([P+](CCCc2ccc(OC3CCCCO3)cc2)(c2ccccc2)c2ccccc2)cc1
[3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromide
O
water
[Li][CH2]CCC
butyllithium
CCCCC[C@H]1CC[C@H](C=CCCc2ccccc2O)CC1
(4-(trans-4-Pentylcyclohexyl)-3-butenyl]phenol

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.STIRRINGThe reaction is stirred a further 30 minutes
  2. 2
    Extraktionextracted with ether
  3. 3
    WaschenThe combined organic layers are washed with brine
  4. 4
    Trocknendried over sodium sulfate
  5. 5
    SonstigeThe solvent is removed in vacuo
  6. 6
    Sonstigechromatographed

Vorschrift

To a solution of [3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromide 3D (R=pentyl) (1.68 g) in tert-butyl methyl ether at room temperature is added, dropwise, a 2.6 M solution of butyllithium (1.25 mL). The orange reaction mixture is stirred for 30 minutes, then a solution of cyclohexanal 3F (R=pentyl) (0.558 g) in tert-butyl methyl ether (3 mL) is added dropwise. The reaction is stirred a further 30 minutes, then poured into water and extracted with ether. The combined organic layers are washed with brine, then dried over sodium sulfate. The solvent is removed in vacuo and the residual material is flash chromatographed using 10% ethyl acetate in hexanes as the eluent.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06413448B1uspto-grants-2002_07