Реакция #41159

ord-00aa65de77f2400c997f6ded7241b20d

Реагенты

Нет

Растворители

Условия реакции

Температура
67.5°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеto precipitate out of solution before the carbazate
  2. 2
    workup.ADDITIONDiluted with additional hexanes
  3. 3
    Температураheated another 15 minutes
  4. 4
    ТемператураThe mixture was cooled to room temperature
  5. 5
    Концентрированиеconcentrated in vacuo
  6. 6
    workup.ADDITIONIsopropanol was added to the residue
  7. 7
    workup.ADDITIONdiluted with ether
  8. 8
    Температураchilled
  9. 9
    ФильтрацияThe solid was collected by filtration
  10. 10
    Другоеdried in vacuo

Методика

Tetrahydro-4H-pyran-4-one (1.002 g, 10.01 mmol, CAS #29943-42-8, purchased from Fluka) was combined with tert-butyl carbazate (1.322 g, 10.00 mmol) in hexanes (10 mL). The mixture was heated in an oil bath at 65-70° C. for 75 minutes. A new precipitate began to precipitate out of solution before the carbazate completely went into solution. The mixture became very thick with the solid precipitate. Diluted with additional hexanes and heated another 15 minutes. The mixture was cooled to room temperature and concentrated in vacuo. Isopropanol was added to the residue and the mixture was stirred vigorously for 5 minutes and then diluted with ether and chilled. The solid was collected by filtration and dried in vacuo to give N′-(tetrahydro-pyran-4-ylidene)-hydrazinecarboxylic acid tert-butyl ester 1.326 g, 62%). A second crop (0.373 g, 17%) was collected from the mother liquor.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07728029B2uspto-grants-2010_06