Water → HCID 22121436, compound
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
- customThe EA phase was removed
- customdried
- concentrationconcentrated
- dissolutionThe residue was dissolved in acetonitrile (50 ml)
- addition2 N sulfuric acid (15 ml) was added to the solution
- waitAfter standing at RT for 1 h
- extractionextracted twice with EA
- washThe EA phase was washed with saturated sodium hydrogencarbonate solution
- customdried
- concentrationconcentrated
- customThe residue was purified
- customwithin 30 min
Sources & evidence
- ORD record
- ord-ecd3236a6b8b45439c275ab36f411dab
- Source dataset
- uspto-grants-2012_06
- Patent number
- US08198272B2
Reaction notes
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