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2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile → (4-Cyano-3,5-difluorophenyl)boronic acid

HRID 2367311
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2367311
[F:1][C:2]1[CH:9]=[C:8]([B:10]2[O:14]C(C)(C)C(C)(C)[O:11]2)[CH:7]=[C:6]([F:19])[C:3]=1[C:4]#[N:5]>CC(C)=O.O>[C:4]([C:3]1[C:2]([F:1])=[CH:9][C:8]([B:10]([OH:14])[OH:11])=[CH:7][C:6]=1[F:19])#[N:5]
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Komponenten

4

Edukt 1

HCID 585045902,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

Produkt 1

HCID 55252910(4-Cyano-3,5-difluorophenyl)boronic acidAusbeute 79 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 180AcetoneLösungsmittelHCID 962WaterLösungsmittel

Versuchsvorschrift

2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile (55 g) was dissolved in acetone (1 L) and water (1 L). T this stirred mixture was added NaIO4 (160 g) and NH4OAc (50 g). The reaction mixture was stirred at room temperature overnight and then filtered. The filtrate was evaporated under vacuum at 40° C. until most of acetone was removed. The residue was cooled to 0° C. and 2N NaOH (1 L) solution was added with stirring over 30 minutes. The mixture was filtered, and the filtrate was washed with CH2Cl2 (1 L). To the aqueous layer was added 5N hydrochloric acid at 0° C. until pH=2. The resulting solid was filtered and then dissolved in EtOAc (1.5 L), dried over Na2SO4, filtered and evaporated under vacuum to provide 30 g of the title compound as a white solid.

Aufarbeitung

  1. filtrationfiltered
  2. customThe filtrate was evaporated under vacuum at 40° C. until most of acetone
  3. customwas removed
  4. temperatureThe residue was cooled to 0° C.
  5. addition2N NaOH (1 L) solution was added
  6. stirringwith stirring over 30 minutes
  7. filtrationThe mixture was filtered
  8. washthe filtrate was washed with CH2Cl2 (1 L)
  9. additionTo the aqueous layer was added 5N hydrochloric acid at 0° C. until pH=2
  10. filtrationThe resulting solid was filtered
  11. dissolutiondissolved in EtOAc (1.5 L)
  12. dry with materialdried over Na2SO4
  13. filtrationfiltered
  14. customevaporated under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-b8b33cce66d0400b9126ec32f496a119
Quelldatensatz
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08697685B2

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