Реакция #41159
ord-00aa65de77f2400c997f6ded7241b20d
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1Другоеto precipitate out of solution before the carbazate
- 2workup.ADDITIONDiluted with additional hexanes
- 3Температураheated another 15 minutes
- 4ТемператураThe mixture was cooled to room temperature
- 5Концентрированиеconcentrated in vacuo
- 6workup.ADDITIONIsopropanol was added to the residue
- 7workup.ADDITIONdiluted with ether
- 8Температураchilled
- 9ФильтрацияThe solid was collected by filtration
- 10Другоеdried 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.