Реакция #1135821

ord-c52d3df7081040d3aace01d7b015d941

Уравнение реакции

Cc1c(O)cccc1O
2-Methylresorcinol
O=C(O)Cc1ccc(O)cc1
4-Hydroxyphenylacetic acid
CCOCC.FB(F)F
BF3.OEt2
Cc1c(O)ccc(C(=O)Cc2ccc(O)cc2)c1O
1-(2,4-Dihydroxy-3-methyl-phenyl)-2-(4-hydroxy-phenyl)-ethanone

Реагенты

Нет

Условия реакции

Температура
110°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe round bottom flask was attached to a condenser
  2. 2
    Другоеplaced in an oil bath
  3. 3
    ДругоеA yellow solid formed at 20 minutes
  4. 4
    workup.WAITThe reaction was left
  5. 5
    Температураon heat for a further 10 minutes
  6. 6
    Температураcooled to room temperature
  7. 7
    ФильтрацияThe yellow solid was collected by suction filtration
  8. 8
    Промывкаwashed with distilled water (200 ml)
  9. 9
    Другоеto remove any excess BF3.OEt2 present
  10. 10
    ДругоеThe solid was dried on a freeze dryer for 24 hours (8.93 g, 99%)

Методика

2-Methylresorcinol (4.00 g, 1 equivalent) and 4-Hydroxyphenylacetic acid (5.00 g, 1 equivalent) were added to a round bottom flask. The round bottom flask was attached to a condenser and placed in an oil bath, the whole system was kept under nitrogen. Distilled BF3.OEt2 (20 ml, 5 equiv.) was added to the mixture while stirring. The mixture was refluxed (110° C.). A yellow solid formed at 20 minutes indicating that the reaction had gone to completion. The reaction was left on heat for a further 10 minutes and then cooled to room temperature. The yellow solid was collected by suction filtration and washed with distilled water (200 ml) to remove any excess BF3.OEt2 present. 1H NMR in d-DMSO indicated the yellow solid was 1-(2,4-Dihydroxy-3-methyl-phenyl)-2-(4-hydroxy-phenyl)-ethanone in >95% purity. The solid was dried on a freeze dryer for 24 hours (8.93 g, 99%).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09381186B2uspto-grants-2016_07