반응 #1135821

ord-c52d3df7081040d3aace01d7b015d941

반응 방정식

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

반응 조건

온도
110°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

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

실험 절차

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%).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09381186B2uspto-grants-2016_07