Реакция #1710841

ord-e29b8f30fcd14c0b88d8cd158ad38912

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONwas added
  2. 2
    Температураthe resulting mixture was refluxed overnight
  3. 3
    ТемператураAfter cooling
  4. 4
    Фильтрацияthe precipitate was filtered
  5. 5
    Другоеthe filtrate was evaporated
  6. 6
    Промывкаwas eluted with hexane/ethyl acetate=4:1

Методика

A mixture of methyl 2,5-dihydroxybenzoate (10 g, 59.5 mmol), potassium carbonate (50.0 g, 362 mmol), and dry acetone (450 ml) was stirred at room temperature for 30 min. 4-Methylbenzenesulfonyl chloride (11.44 g, 60.0 mmol) was added portionwise and the mixture was refluxed for 7 h. (Bromomethyl)benzene (25.4 g, 149 mmol) was added and the resulting mixture was refluxed overnight. After cooling, the precipitate was filtered, and the filtrate was evaporated. The residue was loaded onto a silica gel column and was eluted with hexane/ethyl acetate=4:1 to yield the title compound as a yellow solid. 22 g.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08778939B2uspto-grants-2014_07