Carbon Dioxide → HCID 86685086, compound
Reaction equation
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[C:4]([F:9])[CH:3]=1.[CH:10]([N-]C(C)C)(C)C.[Li+].[C:18](=[O:20])=[O:19]>C1COCC1>[CH3:10][C:6]1[CH:7]=[C:2]([Br:1])[C:3]([C:18]([OH:20])=[O:19])=[C:4]([F:9])[C:5]=1[CH3:8]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- -78 °C
Procedure
To a solution of 4-bromo-2-fluoro-1-methylbenzene (21.9 g, 116 mmol) in THF (100 mL) was added lithium diisopropylamide (LDA) (2 M solution in THF, 69 mL, 139 mmol) at −78° C. After being stirred at −78° C. for 1 h, the reaction was treated with excess solid carbon dioxide, and stirred while the reaction temperature slowly rose to room temperature. The mixture was concentrated and then partitioned between 4N NaOH and ethyl acetate. The aqueous phase was adjusted to pH 2 with 2N HCl and then extracted three times with ethyl acetate. The combined extracts were washed with water and brine, dried over with anhydrous Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel eluted with EA to give methyl 6-bromo-2-fluoro-3-methylbenzoic acid (23.3 g, 86.2%) as a white solid.
Workup
- stirringstirred while the reaction temperature
- customslowly rose to room temperature
- concentrationThe mixture was concentrated
- custompartitioned between 4N NaOH and ethyl acetate
- extractionextracted three times with ethyl acetate
- washThe combined extracts were washed with water and brine
- dry with materialdried over with anhydrous Na2SO4
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by column chromatography on silica gel
- washeluted with EA
Sources & evidence
- ORD record
- ord-12786085893443de8fbc51610aa7f617
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08853186B2
Reaction notes
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