Diiodomethane → 12H-dibenzo[d,g][1,3]dioxocin-12-one

HRID 367251

Reaction equation

HRID 367251 reaction equation
[OH:1][C:2]1[CH:16]=[CH:15][CH:14]=[CH:13][C:3]=1[C:4]([C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=1[OH:12])=[O:5].I[CH2:18]I.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[CH:13]1[C:3]2[C:4](=[O:5])[C:6]3[CH:11]=[CH:10][CH:9]=[CH:8][C:7]=3[O:12][CH2:18][O:1][C:2]=2[CH:16]=[CH:15][CH:14]=1

Participants

5

Conditions

Temperature
105 °C

Procedure

2,2'-Dihydroxybenzophenone (10.0 g, 46.7 mmol) and diiodomethane (13.1 g, 49 mmol) was dissolved in dry N,N-dimethylformamide (180 ml). Dried finely powdered potassium carbonate (9.2 g, 66.7 mmol) was added and the mixture was heated at 105° C. for 16 h. After cooling to room temperature the reaction mixture was poured into ice water (500 ml). The precipitate was collected by filtration after 0.5 h, washed with water on the filter and dissolved in a mixture of ethanol (80 ml) and 4 N sodium hydroxide (20 ml). The solution was stirred at reflux temperature for 1 h, cooled and diluted with water (300 ml). The formed crystalline precipitate was filtered off, washed with water (50 ml) and dried in vacuo, affording 12H-dibenzo[d,g][1,3]dioxocin-12-one as a solid (9.5 g, 90%).

Workup

  1. additionwas added
  2. temperatureAfter cooling to room temperature the reaction mixture
  3. filtrationThe precipitate was collected by filtration after 0.5 h
  4. washwashed with water on the
  5. filtrationfilter
  6. dissolutiondissolved in a mixture of ethanol (80 ml) and 4 N sodium hydroxide (20 ml)
  7. temperatureat reflux temperature for 1 h
  8. temperaturecooled
  9. additiondiluted with water (300 ml)
  10. filtrationThe formed crystalline precipitate was filtered off
  11. washwashed with water (50 ml)
  12. customdried in vacuo

Sources & evidence

ORD record
ord-49e1adac2c794d6dab7302e1aef7c6f0
Source dataset
uspto-grants-2000_10
Patent number
US06133268

Linked notes

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