Реакция #2122505

ord-062d06ec7c0f4a818b9ef68c5e7b26f6

Уравнение реакции

CC(C)(C)O
tert-butyl alcohol
O=C(O)c1cc(O)ccc1O
2,5-dihydroxybenzoic acid
O=S(=O)(O)O
sulfuric acid
CC(C)(C)O
tert-butyl alcohol
O=C(O)c1ccccc1O
salicylic acid
Выход 83.6%

Растворители

Условия реакции

Температура
50°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    workup.ADDITIONmixed
  2. 2
    ДругоеTo the liquid dispersion obtained
  3. 3
    workup.STIRRINGthe mixture was stirred for 30 minutes
  4. 4
    ДругоеThe reaction solution obtained
  5. 5
    Температураwas cooled to room temperature
  6. 6
    Другоеformed
  7. 7
    Фильтрацияwas filtered
  8. 8
    Промывкаwhich was then washed with water
  9. 9
    Промывкаfurther washed with hexane
  10. 10
    ДругоеThe precipitate formed
  11. 11
    Другоеthe solution obtained
  12. 12
    Другоеwas re-precipitated in 3.6 L of water
  13. 13
    ФильтрацияAfter filtration
  14. 14
    Другоеthe product was dried at 80° C.

Методика

100 g of 2,5-dihydroxybenzoic acid and 1,441 g of 80% sulfuric acid were heated to 50° C. and mixed. To the liquid dispersion obtained, 144 g of tert-butyl alcohol was added, and the mixture was stirred at 50° C. for 30 minutes. Thereafter, the operation that 144 g of tert-butyl alcohol was added to the liquid dispersion and the mixture was stirred for 30 minutes was carried out three times. The reaction solution obtained was cooled to room temperature, and then dropwise added to 1 kg of ice water, where the precipitate formed was filtered, which was then washed with water and further washed with hexane. The precipitate formed was dissolved in 200 mL of methanol, and the solution obtained was re-precipitated in 3.6 L of water. After filtration, the product was dried at 80° C. to obtain 74.9 g of a salicylic acid intermediate represented by the following formula (3).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08574801B2uspto-grants-2013_11