تفاعل #1135826

ord-7582fee70f034cfd8de9a9cf5a5e2a4f

معادلة التفاعل

Cc1c(O)cccc1O
2-Methylresorcinol
COc1ccc(CC(=O)O)cc1OC
3,4-dimethoxyphenylacetic acid
CCOCC.FB(F)F
boron trifluoride diethyl etherate
CCOCC.FB(F)F
BF3.OEt2
COc1ccc(CC(=O)c2ccc(O)c(C)c2O)cc1OC
1-(2,4-dihydroxy-3-methyl-phenyl)-2-(3,4-dimethoxy-phenyl) ethanone

ظروف التفاعل

درجة الحرارة
110°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe round bottom flask was attached to a condenser
  2. 2
    أخرىplaced in an oil bath
  3. 3
    أخرىA yellow solid formed at 75 minutes
  4. 4
    درجة الحرارةThe reaction was heated for a further 10 minutes
  5. 5
    درجة الحرارةcooled to room temperature
  6. 6
    ترشيحThe yellow solid was collected by suction filtration
  7. 7
    غسيلwashed with distilled water (200 ml)
  8. 8
    أخرىto remove any excess BF3.OEt2 present
  9. 9
    أخرىThe solid was dried on a freeze dryer for 24 hours (6.303 g, 43%)

الإجراء التجريبي

2-Methylresorcinol (6.285 g, 1 equivalent) and 3,4-dimethoxyphenylacetic acid (9.251 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 boron trifluoride diethyl etherate, BF3.OEt2 (42 ml, 5 equiv.) was added to the mixture while stirring. The mixture was refluxed (110° C.). A yellow solid formed at 75 minutes indicating that the reaction had gone to completion. The reaction was heated for a further 10 minutes and 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-(3,4-dimethoxy-phenyl) ethanone in >95% purity. The solid was dried on a freeze dryer for 24 hours (6.303 g, 43%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09381186B2uspto-grants-2016_07