Reaktion #2314290
ord-d061030504034931b997d04d806f93a4
Reaktionsgleichung
cyclohexanal
4-Pentylcyclohexanal
[3-(4-[2-Tetrahydropyranyloxy]phenyl)propyl]triphenylphosphonium bromide
water
butyllithium
→
(4-(trans-4-Pentylcyclohexyl)-3-butenyl]phenol
Edukte
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1workup.STIRRINGThe reaction is stirred a further 30 minutes
- 2Extraktionextracted with ether
- 3WaschenThe combined organic layers are washed with brine
- 4Trocknendried over sodium sulfate
- 5SonstigeThe solvent is removed in vacuo
- 6Sonstigechromatographed
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.