Реакция #2389083

ord-b2423c17d13b4b37a9bab7a26b342176

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONadded dropwise by syringe
  2. 2
    workup.ADDITIONthe addition
  3. 3
    workup.STIRRINGthe reaction was stirred at room temperature for 4 hours
  4. 4
    ДругоеThe solvent was evaporated under vacuum and ether (30 mL)
  5. 5
    workup.ADDITIONwas added
  6. 6
    Другоеto precipitate the triphenylphosphine oxide and hydrazine dicarboxylate which
  7. 7
    Другоеwere removed by filtration
  8. 8
    ПромывкаThe precipitate was rinsed with ether (2×30 mL)
  9. 9
    Другоеthe combined filtrates were evaporated
  10. 10
    Другоеto afford a yellow solid
  11. 11
    ДругоеThe yellow solid was triturated with warm hexanes (3×50 mL)
  12. 12
    Фильтрацияfiltered
  13. 13
    ДругоеThe combined hexanes were evaporated

Методика

A mixture of 10-undecene-1-ol (5.00 g, 29.36 mmol, 1 equiv), triphenylphosphine (7.70 g, 29.36 mmol, 1 equiv) and phthalimide (4.32 g, 29.36 mmol, 1 equiv) in dry tetrahydrofuran (THF, 30 mL) was stirred vigorously under argon. Diethyl azodicarboxylate (DEAD, 5.11 g, 29.36 mmol, 1 equiv) was diluted with THF (12 mL) and added dropwise by syringe. After; the addition, the reaction was stirred at room temperature for 4 hours. The solvent was evaporated under vacuum and ether (30 mL) was added to precipitate the triphenylphosphine oxide and hydrazine dicarboxylate which were removed by filtration. The precipitate was rinsed with ether (2×30 mL) and the combined filtrates were evaporated to afford a yellow solid. The yellow solid was triturated with warm hexanes (3×50 mL) and filtered. The combined hexanes were evaporated to give 1-phthalimidylundec-10-ene as a yellow wax.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US06428780B2uspto-grants-2002_08