Реакция #429504

ord-ca8534a1906f46efa1363e478d827682

Реагенты

Нет

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеAfter the reaction
  2. 2
    Экстракцияsubjected to extraction with toluene
  3. 3
    Промывкаby washing successively with 5%-hydrochloric acid aqueous solution and water
  4. 4
    Сушкаdrying with anhydrous magnesium sulfate
  5. 5
    ФильтрацияThe resultant organic layer was subjected to filtration

Методика

8.0 g of 4-n-pentylcyclohexylmethanol was dissolved in a mixture solvent of 8 ml of pyridine and 8 ml of toluene. To the solution, 6.0 g of methanesulfonyl chloride was added dropwise below 10° C., followed by stirring overnight at room temperature. After the reaction, the reaction mixture was poured into cold water and subjected to extraction with toluene, followed by washing successively with 5%-hydrochloric acid aqueous solution and water and drying with anhydrous magnesium sulfate. The resultant organic layer was subjected to filtration, followed by distilling-off of the solvent to obtain 11.3 g of 4-n-pentylcyclohexylmethyl methanesulfonate.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US05858269uspto-grants-1999_01