Iodine → 2-(2-Fluoro-3-iodo-4-methoxy-phenyl)-[1,3] dioxolane
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[CH:10]1[O:14][CH2:13][CH2:12][O:11]1.[Li]CCCC.[I:20]I>C1COCC1>[F:1][C:2]1[C:7]([I:20])=[C:6]([O:8][CH3:9])[CH:5]=[CH:4][C:3]=1[CH:10]1[O:11][CH2:12][CH2:13][O:14]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
To a solution of 2-(2-fluoro-4-methoxy-phenyl)-[1,3] dioxolane (4.27 g, 21.54 mmol) in anhydrous THF (30 mL) was added, at −78° C. under argon, n-BuLi (1.6 M in hexane, 13.5, 21.54 mmol). The resulting orange solution was stirred at −78° C. for 2 hours then iodine (6.015 g, 23.70 mmol) in THF (30 mL) was added. At the end of the addition the reaction mixture was warmed to room temperature and stirred for 1 hr. The solution was extracted with ethyl acetate. The organic phase was washed successively with 10% aqueous sodium thiosulfate (2×50 mL), water, brine and dried (MgSO4), filtered and evaporated to give 5.794 g of crude 2-(2-fluoro-3-iodo-4-methoxy-phenyl)-[1,3] dioxolane. use as this in the next step.
Workup
- additionAt the end of the addition the reaction mixture
- temperaturewas warmed to room temperature
- stirringstirred for 1 hr
- extractionThe solution was extracted with ethyl acetate
- washThe organic phase was washed successively with 10% aqueous sodium thiosulfate (2×50 mL), water, brine
- dry with materialdried (MgSO4)
- filtrationfiltered
- customevaporated
Sources & evidence
- ORD record
- ord-95f392cd88d447e085305e47442bfde5
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07102000B2
Reaction notes
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