Реакция #2439930

ord-45fda99b4fb8441b8a76d1bb712b702c

Уравнение реакции

CCCCC
pentane
C=CC(O)C/C=C\C/C=C\CC
(5Z,8Z)-1,5,8-undecatrien-3-ol
CN(C)P(=O)(N(C)C)N(C)C
hexamethylphosphoric triamide
C[P+](Oc1ccccc1)(Oc1ccccc1)Oc1ccccc1.[I+]
methyl(triphenoxy)phosphonium iodine
C=C/C=C/C=C/C/C=C\CC
(3E,5E,8Z)-1,3,5,8-undecatetraene
Выход 20.0%
C=C/C=C/C=C\C/C=C\CC
(3E,5Z,8Z)-1,3,5,8-undecatetraene
Выход 20.0%

Растворители

Условия реакции

Температура
50°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Экстракцияby extracting with pentane
  2. 2
    ПромывкаAfter the organic layer was washed with a saturated aqueous sodium chloride solution, it
  3. 3
    Сушкаwas dried over anhydrous magnesium sulfate
  4. 4
    ДругоеAfter evaporation of the solvent
  5. 5
    Другоеto give 2.0 g (yield: 74%) of a crude product

Методика

(5Z,8Z)-1,5,8-undecatrien-3-ol (3.0 g, 18.1 mmol), 60 ml of hexamethylphosphoric triamide (HMPTA) and 16.4 g (36.2 mmol) of methyl(triphenoxy)phosphonium iodine (MTPI) were added to a reactor under a nitrogen atmosphere followed by stirring at room temperature for 3 hours and at 50° C. for 1 hour. The reaction was stopped by addition of 50 ml of ice water followed by extracting with pentane. After the organic layer was washed with a saturated aqueous sodium chloride solution, it was dried over anhydrous magnesium sulfate. After evaporation of the solvent, the resulting residue was subjected to a chromatographic treatment using pentane to give 2.0 g (yield: 74%) of a crude product. The resultant crude product (0.5 g, 3.37 mmol) was further purified by a chromatography using pentane and diethyl ether to give 0.05 g (yield: 20%) of (3E,5Z,8Z)-1,3,5,8-undecatetraene and 0.05 g (yield: 20%) of (3E,5E,8Z)-1,3,5,8-undecatetraene.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07749551B2uspto-grants-2010_07