تفاعل #7821

ord-8e21f0f9208d4b068d738415af301ac5

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISSOLUTIONto help dissolve solids
  2. 2
    أخرىin reaction mixture
  3. 3
    أخرىreaction mixture
  4. 4
    workup.STIRRINGstir overnight at rt
  5. 5
    غسيلby washing
  6. 6
    أخرىreaction
  7. 7
    استخلاصwith brine (3×30 mL), extraction with EtOAc
  8. 8
    تجفيفdried (Na2SO4)
  9. 9
    ترشيحfiltered
  10. 10
    أخرىremoved solvent in vacuo
  11. 11
    أخرىFlash chromatography of resulting orange solid on silica gel using
  12. 12
    غسيلa gradient elution of 1:9 EtOAc

الإجراء التجريبي

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 yellow solid. 1H NMR(CDCl3, 300 MHz) δ 7.86–7.36 (m, 7H), 3.99 (s, 3H), 3.74 (s, 2H), 2.59–1.91 (m, 8H). MS (ESI) 265 (M+H)+.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07087601B2uspto-grants-2006_08