Reaktion #7829

ord-4d49f2de2fea4e568118fe4805b7b8f7

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.DISSOLUTIONto help dissolve solids
  2. 2
    Sonstigein reaction mixture
  3. 3
    Sonstigereaction mixture
  4. 4
    workup.STIRRINGstir overnight at rt
  5. 5
    Waschenby washing
  6. 6
    Sonstigereaction
  7. 7
    Extraktionwith brine (3×30 mL), extraction with EtOAc
  8. 8
    Trocknendried (Na2SO4)
  9. 9
    Filtrationfiltered
  10. 10
    Sonstigeremoved solvent in vacuo
  11. 11
    SonstigeFlash chromatography of resulting orange solid on silica gel using
  12. 12
    Waschena gradient elution of 1:9 EtOAc

Vorschrift

A mixture of, 2-[4-(bromomethyl)-3-methoxyphenyl]-1,3-benzoxazole (318 mg, 1 mmol), dimethylformamide (7.5 mL) and deionzed water (2.5 mL) was stirred at rt. Sodium cyanide (150 mg, 3.0 mmol) was added to reaction. After 3 h, dimethylformamide (10 mL) was added to help dissolve solids in reaction mixture. Let reaction mixture stir overnight at rt. Workup was done by washing reaction with brine (3×30 mL), extraction with EtOAc, combined organic extracts, dried (Na2SO4), filtered and removed solvent in vacuo. Flash chromatography of resulting orange solid on silica gel using a gradient elution of 1:9 EtOAc:hexanes to 1:3 EtOAc:hexanes afforded the desired intermediate, [4-(1,3-benzoxazol-2-yl)-2-methoxyphenyl]acetonitrile, as a light yellow solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07087601B2uspto-grants-2006_08