Iodide Ion → HCID 57692979, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[CH:4][C:3]=1[C:12]1[CH:17]=[CH:16][C:15]([O:18][CH3:19])=[CH:14][C:13]=1[F:20].[I-:21].OS([O-])=O.[Na+]>S([O-])([O-])(=O)=O.[Ag+2].CO>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([O:10][CH3:11])=[O:9])[CH:5]=[CH:4][C:3]=1[C:12]1[CH:17]=[C:16]([I:21])[C:15]([O:18][CH3:19])=[CH:14][C:13]=1[F:20]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
methyl 2-chloro-2′-fluoro-4′-methoxybiphenyl-4-carboxylate (550 mg, 1.87 mmol), methanol (8 mL), iodide (474 mg, 1.87 mmol) and silver sulfate (583 mg, 1.87 mmol) were stirred at room temperature for 2 hours. Reaction crude was worked up with NaHSO3 (aq). Volatiles were removed under reduced pressure. The pot residue was worked up with brine, extracted with ethyl acetate, dried over Na2SO4, filtered and evaporated to afford a light brown solid. This solid was purified by SiO2 (Biotage Horizon Flash system, 40+M cartridge, 0-20% EtOAc/hexanes, v/v) to afford the title compound. LCMS (ESI) calc.=419.94; found=420.86 (M+1)+.
Workup
- customReaction crude
- customVolatiles were removed under reduced pressure
- extractionextracted with ethyl acetate
- dry with materialdried over Na2SO4
- filtrationfiltered
- customevaporated
- customto afford a light brown solid
- customThis solid was purified by SiO2 (Biotage Horizon Flash system, 40+M cartridge, 0-20% EtOAc/hexanes
Sources & evidence
- ORD record
- ord-d7ee7cf6a7b74510b1513d7c98d58e72
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08440702B2
Reaction notes
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