Hydrochloric Acid → HCID 131735406, compound

Temperature

5 °C

In a nitrogen atmosphere, metal magnesium (3.9 g) was suspended in THF (5 mL), a solution prepared by dissolving 4-bromo-3-fluoroanisole (30 g) in THF (150 mL) was added at a rate at which the solution was gently refluxed, and stirring was performed at 40° C. for one hour. Subsequently, the reaction liquid was cooled to 5° C. After a solution prepared by dissolving trimethyl borate (19.8 g) in THF (60 mL) was added thereto, stirring was performed at room temperature for one hour. Toluene (150 mL) and 10% hydrochloric acid (100 mL) were added thereto and the mixture was separated. Toluene (100 mL) was added to the resulting aqueous layer and extraction was performed. The obtained organic layers were mixed and washed with a saturated saline solution (100 mL). Anhydrous sodium sulfate was added to perform drying, and the organic solvent was distilled off under reduced pressure. Thus, a crude 2-fluoro-4-methoxyphenylboric acid (26.3 g) was obtained. (3-2) In a nitrogen atmosphere, 5,6,7-trifluoro-2-naphthol (30 g) and pyridine (15.6 g) were dissolved in dichloromethane (150 mL) and cooled to 5° C., and a solution prepared by dissolving trifluoromethanesulfonic acid anhydride (47.0 g) in dichloromethane (150 mL) was added thereto. After stirring was performed at room temperature for one hour, water (200 mL) was added and the mixture was separated. The resulting organic layer was washed with 10% hydrochloric acid (150 mL), an aqueous saturated sodium hydrogen carbonate solution (150 mL), and a saturated saline solution (150 mL). Anhydrous sodium sulfate was added to perform drying, and the organic solvent was distilled off under reduced pressure. Purification was performed by silica gel column chromatography to obtain 5,6,7-trifluoro-2-naphthyl trifluoromethanesulfonate (49.4 g). (3-3) In a nitrogen atmosphere, the 5,6,7-trifluoro-2-naphthyl trifluoromethanesulfonate obtained in (3-2) (40.0 g), tetrakis(triphenylphosphine)palladium (0) (1.4 g), a 2 mol/L aqueous potassium carbonate solution (120 mL), and THF (200 mL) were mixed with each other and heated to 60° C. A solution prepared by dissolving 2-fluoro-4-methoxyphenylboric acid (24.7 g) obtained in (3-1) in THF (100 mL) was added thereto, and stirring was performed at 60° C. for six hours. The temperature was decreased to room temperature. Toluene (150 mL) was added thereto and the mixture was separated. The resulting organic layer was washed with water (100 mL) and a saturated saline solution (100 mL). Anhydrous sodium sulfate was added to perform drying, and the organic solvent was distilled off under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain a crude 2-(2-fluoro-4-methoxyphenyl)-5,6,7-trifluoronaphthalene (35.1 g). (3-4) The crude 2-(2-fluoro-4-methoxyphenyl)-5,6,7-trifluoronaphthalene (35.1 g) obtained in (3-3) was dissolved in dichloromethane (350 mL) and cooled to 5° C., and boron tribromide (14.4 g) was added thereto. After stirring was performed at room temperature for three hours, the temperature was decreased to 5° C. Water (100 mL) was added thereto and the mixture was separated. The resulting organic layer was washed with a saturated saline solution (100 mL) twice. Anhydrous sodium sulfate was added to perform drying, and the organic solvent was distilled off under reduced pressure. The resulting residue was purified by alumina column chromatography and recrystallized using hexane to obtain 4-(5,6,7-trifluoro-2-naphthyl)-3-fluorophenol (25.3 g). (3-5) The subsequent processes were performed by the same method as in Example 1 to obtain [3,5-difluoro-4-(2-fluoro-4-(trans-4-propylcyclohexyl)phenyl)phenyl]-[3-fluoro-4-(5,6,7-trifluoro-2-naphthyl)phenyloxy]difluoromethane (49.9 g).

1. customa solution prepared
2. additionwas added at a rate at which the solution
3. temperaturewas gently refluxed
4. customSubsequently, the reaction liquid
5. customAfter a solution prepared
6. additionwas added
7. stirringstirring
8. waitwas performed at room temperature for one hour
9. customthe mixture was separated
10. additionToluene (100 mL) was added to the resulting aqueous layer and extraction
11. additionThe obtained organic layers were mixed
12. washwashed with a saturated saline solution (100 mL)
13. additionAnhydrous sodium sulfate was added
14. customto perform drying
15. distillationthe organic solvent was distilled off under reduced pressure

ORD record

ord-5d923ca879b84757b65ac91ebd0f8523

Source dataset

uspto-grants-2016_04

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US09315727B2