반응 #65265

ord-36b0a4d7b9a846cf893de012bb3b71a0

반응 방정식

O=N[O-].[Na+]
sodium nitrite
F[B-](F)(F)F.[H+]
Fluoroboric acid
CCCCc1nc(N)c(C(=O)OCC)n1Cc1ccccc1Cl
2-n-butyl-1-{(2-chlorophenyl)methyl}-4-amino-5-carboethoxyimidazole
CCCCc1nc(F)c(C(=O)OCC)n1Cc1ccccc1Cl
2-n-butyl-1-{(2-chlorophenyl)methyl}-4-fluoro-5-carboethoxyimidazole

용매

반응 조건

온도
0°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The resulting solid mass was sonicated
  2. 2
    기타to form a suspension
  3. 3
    기타The ice bath was removed
  4. 4
    기타the reaction mixture was irradiated for 20 hours with a 450-watt mercury vapor lamp
  5. 5
    온도cooled
  6. 6
    온도The reaction mixture was cooled to -20° C.
  7. 7
    추출The product was extracted into ethyl acetate (3×)
  8. 8
    세척the combined extracts were washed with water and saturated sodium chloride solution
  9. 9
    추출The organic extract
  10. 10
    건조was dried with anhydrous sodium sulfate
  11. 11
    농축concentrated
  12. 12
    기타to give 8.43 g of a crude product, which
  13. 13
    기타was chromatographed on silica gel eluting with chloroform

실험 절차

The 4-amino product was fluorinated using the procedure of K. L. Kirk and L. J. Cohen, JACS, 95 (14), 4619 (1973). Fluoroboric acid (48%, 150 mL) was added to 2-n-butyl-1-{(2-chlorophenyl)methyl}-4-amino-5-carboethoxyimidazole (10.75 g, 0.032 mol) in a quartz flask. The resulting solid mass was sonicated and stirred vigorously to form a suspension. This suspension was cooled to 0° C. and then sodium nitrite (2.80 g, 0.0406 mol) in 5 mL of water was added slowly. The ice bath was removed and then the reaction mixture was irradiated for 20 hours with a 450-watt mercury vapor lamp placed in a quartz immersion well, cooled by circulating water. The reaction mixture was cooled to -20° C. and the pH was adjusted to 6.4 with 50% aqueous sodium hydroxide. The product was extracted into ethyl acetate (3×) and the combined extracts were washed with water and saturated sodium chloride solution. The organic extract was dried with anhydrous sodium sulfate and concentrated to give 8.43 g of a crude product, which was chromatographed on silica gel eluting with chloroform to give 4.31 g of 2-n-butyl-1-{(2-chlorophenyl)methyl}-4-fluoro-5-carboethoxyimidazole.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05418250uspto-grants-1995_05