تفاعل #1929065

ord-722fec5ad5834279baaecd9e644e66c8

معادلة التفاعل

OB(O)c1ccc(Cl)c(F)c1
(4-chloro-3-fluorophenyl)boronic acid
Cc1ccc(Br)cc1CC(=O)O
(5-bromo-2-methylphenyl)acetic acid
[Na+].[OH-]
sodium hydroxide
CC(C)(C)[PH+](C(C)(C)C)C(C)(C)C.F[B-](F)(F)F
tri-tert-butylphosphonium tetrafluoroborate
Cl
hydrogen chloride
Cc1ccc(-c2ccc(Cl)c(F)c2)cc1CC(=O)O
(4′-Chloro-3′-fluoro-4-methylbiphenyl-3-yl)acetic acid

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.STIRRINGthe mixture was stirred at room temperature for 20 h
  2. 2
    workup.STIRRINGthe mixture was stirred for 10 minutes
  3. 3
    أخرىthe phases were separated
  4. 4
    استخلاصthe aqueous phase was extracted twice with toluene
  5. 5
    تجفيفthe combined organic phases were dried over sodium sulfate
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated
  8. 8
    workup.STIRRINGThe residue was stirred in 300 ml of a 6/1 mixture of n-hexane/tert-butyl methyl ether for 30 minutes
  9. 9
    ترشيحfiltered off with suction
  10. 10
    غسيلwashed with n-hexane
  11. 11
    أخرىdried 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08946124B2uspto-grants-2015_02