Реакция #75433

ord-6138fbfac24d447199213a4fb085e741

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONadded dropwise by syringe
  2. 2
    workup.ADDITIONAfter the 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: US06699467B2uspto-grants-2004_03