3-Bromo-4-(trifluoromethoxy)benzoic acid → 1261753-62-1
Reaction equation
Br[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][C:12]([F:15])([F:14])[F:13])[C:5]([OH:7])=[O:6].[CH3:16][Zn]C>O1CCOCC1.C1(C)C=CC=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.C1C=CC(P(C2C=CC=CC=2)[C-]2C=CC=C2)=CC=1.Cl[Pd]Cl.[Fe+2]>[CH3:16][C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][C:10]=1[O:11][C:12]([F:15])([F:14])[F:13])[C:5]([OH:7])=[O:6]Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
A mixture of 3-bromo-4-(trifluoromethoxy)benzoic acid (923 mg, 3.24 mmol) and PdCl2(dppf) (95 mg, 0.13 mmol) were stirred in 1,4-dioxane (9 mL) in a three necked flask under argon atmosphere (a condenser was added to the flask). Dimethylzinc in toluene (3.2 mL of 2.0 M, 6.4 mmol) was added very slowly (caution: the reaction was very exothermic) and the mixture was stirred at room temperature for 1 hour before it was heated at 70° C. for 18 h. The mixture was cooled to room temperature before it was charged with additional dioxane (9 mL) and PdCl2(dppf) (100 mg). The mixture was cooled to 0° C. before additional dimethyl zinc in toluene (3.0 mL, 2.0M) was added. The ice bath was removed and the mixture was heated at 70° C. overnight. The mixture was cooled to room temperature and was quenched with methanol (2 mL) very slowly. The solution was diluted with ethyl acetate and was washed with 1N HCl (3×). The organic layer was washed with brine, dried over sodium sulfate and evaporated to dryness to yield 3-methyl-4-(trifluoromethoxy)benzoic acid (56%).
Workup
- additionwas added to the flask)
- temperaturewas heated at 70° C. for 18 h
- temperatureThe mixture was cooled to room temperature before it
- additionwas added
- customThe ice bath was removed
- temperaturethe mixture was heated at 70° C. overnight
- temperatureThe mixture was cooled to room temperature
- customwas quenched with methanol (2 mL) very slowly
- additionThe solution was diluted with ethyl acetate
- washwas washed with 1N HCl (3×)
- washThe organic layer was washed with brine
- dry with materialdried over sodium sulfate
- customevaporated to dryness
Sources & evidence
- ORD record
- ord-d35dbf15cfb541faabdf91f9e07d7646
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08598164B2
Reaction notes
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