Water → HCID 22121436, compound

HRID 217714Notes

Reaction equation

HRID 217714 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:10](=[O:12])[CH3:11])[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1.[Br-:13].[Br-].[Br-].C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.C1([N+](C)(C)C)C=CC=CC=1.O.CC(=O)OCC>CO.C1COCC1>[Br:13][CH2:11][C:10]([C:4]1[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=[C:2]([Br:1])[CH:3]=1)=[O:12]

Participants

6

Procedure

1-(3-Bromo-5-methoxyphenyl)ethanone (O2.032, 1.45 g) was dissolved in methanol/THF (40 ml/40 ml) and admixed while stirring with phenyltrimethylammonium tribromide (2.38 g). After stirring at RT for 24 h, water and EA were added. The EA phase was removed, dried and concentrated. The residue was dissolved in acetonitrile (50 ml), and 2 N sulfuric acid (15 ml) was added to the solution. After standing at RT for 1 h, the mixture was admixed with water and extracted twice with EA. The EA phase was washed with saturated sodium hydrogencarbonate solution, dried and concentrated. The residue was purified using silica gel (40 g cartridge, n-heptane/EA gradient of 0-50% within 30 min. 1.39 g of the title compound were obtained.

Workup

  1. customThe EA phase was removed
  2. customdried
  3. concentrationconcentrated
  4. dissolutionThe residue was dissolved in acetonitrile (50 ml)
  5. addition2 N sulfuric acid (15 ml) was added to the solution
  6. waitAfter standing at RT for 1 h
  7. extractionextracted twice with EA
  8. washThe EA phase was washed with saturated sodium hydrogencarbonate solution
  9. customdried
  10. concentrationconcentrated
  11. customThe residue was purified
  12. customwithin 30 min

Sources & evidence

ORD record
ord-ecd3236a6b8b45439c275ab36f411dab
Source dataset
uspto-grants-2012_06
Patent number
US08198272B2

Reaction notes

Loading…