Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Trifluoromethyl)phenol | HCID 67874 | — |
| Reactant | HCID 68634494 | HCID 68634494 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86594835 | HCID 86594835 | — |
Reaction Steps
6.8 mg of Methyl [3′-(3-bromo-1-propynyl)-4′-methoxybiphenyl-3-yl acetate was dissolved in 0.2 ml of N,N-dimethylformamide, 10 mg of 4-trifluoromethylphenol and 10 mg of potassium carbonate were added thereto, and the mixture was stirred at room temperature for 3 days. The reaction mixture was diluted with ethyl acetate and washed with water. The organic layer was concentrated to give methyl {4′-methoxy-3′-[3-(4-trifluoromethylphenoxy)-1-propynyl]biphenyl-3-yl}acetate. This product was dissolved in 0.4 ml of ethanol, then 0.1 ml of 5N aqueous sodium hydroxide was added thereto, and the mixture was stirred overnight at room temperature. 1N hydrochloric acid was added to the reaction mixture which was then extracted with ethyl acetate. The organic layer was concentrated, and the residue was purified by reverse-phase high performance liquid chromatography to give 4.89 mg of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07687664B2 |
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| Source dataset | uspto-grants-2010_03 |
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| ORD ID | ord-a565d6e2c35547f598689544d88411b4 |
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| Source note | uspto-grants-2010_03 |
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