تفاعل #2314290

ord-d061030504034931b997d04d806f93a4

معادلة التفاعل

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

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGThe reaction is stirred a further 30 minutes
  2. 2
    استخلاصextracted with ether
  3. 3
    غسيلThe combined organic layers are washed with brine
  4. 4
    تجفيفdried over sodium sulfate
  5. 5
    أخرىThe solvent is removed in vacuo
  6. 6
    أخرىchromatographed

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06413448B1uspto-grants-2002_07