تفاعل #1929065
ord-722fec5ad5834279baaecd9e644e66c8
معادلة التفاعل
المتفاعلات
المذيبات
ظروف التفاعل
المعالجة
- 1workup.STIRRINGthe mixture was stirred at room temperature for 20 h
- 2workup.STIRRINGthe mixture was stirred for 10 minutes
- 3أخرىthe phases were separated
- 4استخلاصthe aqueous phase was extracted twice with toluene
- 5تجفيفthe combined organic phases were dried over sodium sulfate
- 6ترشيحfiltered
- 7تركيزconcentrated
- 8workup.STIRRINGThe residue was stirred in 300 ml of a 6/1 mixture of n-hexane/tert-butyl methyl ether for 30 minutes
- 9ترشيحfiltered off with suction
- 10غسيلwashed with n-hexane
- 11أخرىdried under reduced pressure
الإجراء التجريبي
Under argon, 33.5 g (192 mmol) of (4-chloro-3-fluorophenyl)boronic acid were added to a solution of 40.0 g (175 mmol) of (5-bromo-2-methylphenyl)acetic acid (EP 1791816 and WO 2006/29799) in a mixture of 437 ml (437 mmol) of degassed 1N aqueous sodium hydroxide solution, 160 ml of degassed water and 160 ml of degassed tetrahydrofuran. The mixture was stirred for 10 minutes, 507 mg (1.75 mmol) of tri-tert-butylphosphonium tetrafluoroborate and 532 mg (1.75 mmol) of palladium(II) acetylacetonate were added and the mixture was stirred at room temperature for 20 h. Toluene and water were then added, the pH was adjusted to 1-2 with concentrated aqueous hydrogen chloride solution, the mixture was stirred for 10 minutes, the phases were separated, the aqueous phase was extracted twice with toluene and the combined organic phases were dried over sodium sulfate, filtered and concentrated. The residue was stirred in 300 ml of a 6/1 mixture of n-hexane/tert-butyl methyl ether for 30 minutes, filtered off with suction, washed with n-hexane and dried under reduced pressure. This gave 38.0 g (78% of theory) of the title compound.