Sodium Carbonate → Tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4](B(O)O)[CH:5]=[CH:6][CH:7]=1.C(=O)([O-])[O-].[Na+].[Na+].[C:17]([NH:25][C:26]1[CH:38]=[C:37](Br)[CH:36]=[CH:35][C:27]=1[C:28]([O:30][C:31]([CH3:34])([CH3:33])[CH3:32])=[O:29])(=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>[Pd+2].C1(P(C2CCCCC2)C2C=CC=CC=2)CCCCC1.CN(C)C(=O)C>[C:17]([NH:25][C:26]1[CH:38]=[C:37]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([Cl:1])[CH:3]=2)[CH:36]=[CH:35][C:27]=1[C:28]([O:30][C:31]([CH3:33])([CH3:34])[CH3:32])=[O:29])(=[O:24])[C:18]1[CH:19]=[CH:20][CH:21]=[CH:22][CH:23]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Conditions
- Temperature
- 90 °C
Procedure
44 mp of 3-chlorophenylboronic acid, 49 mg of sodium carbonate and 6 mg of polymer supported di(acetato)dicyclohexylphenylphosphine palladium(II) were added to 2.5 mL of N,N-dimethylacetamide solution containing 70 mg of tert-butyl 2-(benzamido)-4-bromobenzoate, and stirred at 90° C. for 15 hours. After the reaction mixture was cooled to room temperature, 5.1 mg of polymer supported di(acetato) dicyclohexylphenylphosphine palladium(II) was added and stirred at 110° C. for 9 hours and 30 minutes. After the reaction mixture was cooled to room temperature, insoluble were removed by filtration and ethyl acetate and 10% citric acid aqueous solution were added. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with 10% citric acid aqueous solution and a saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [Flash Tube 2008 manufactured by Tribonex Company, eluent; hexane:ethyl acetate=4:1] to obtain tert-butyl 2-(benzamido)-4-(3-chlorophenyl)benzoate.
Workup
- temperatureAfter the reaction mixture was cooled to room temperature
- additionwas added
- stirringstirred at 110° C. for 9 hours and 30 minutes
- temperatureAfter the reaction mixture was cooled to room temperature
- custominsoluble were removed by filtration and ethyl acetate and 10% citric acid aqueous solution
- additionwere added
- customThe organic layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- washafter washed with 10% citric acid aqueous solution
- customa saturated sodium chloride aqueous solution sequentially, and the solvent was evaporated under reduced pressure
- customThe obtained residue was purified with silica gel column chromatography [Flash Tube 2008 manufactured by Tribonex Company, eluent; hexane:ethyl acetate=4:1]
Sources & evidence
- ORD record
- ord-4cbafd099ab44f56adacf567cc1c12ba
- Source dataset
- uspto-grants-2011_08
- Patent number
- US07999132B2
Reaction notes
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