반응 #44750

ord-03b69632e05d43b99ef967c7144e40bf

반응 방정식

CC(=O)Oc1ccc(C(=O)Cl)cc1
4-(chlorocarbonyl)phenyl acetate
C[Si](C)(C)n1nccn1
2-TMS-1,2,3-triazole
CC(=O)Oc1ccc(-c2ncco2)cc1
4-(2-oxazolyl)phenyl acetate

용매

반응 조건

온도
150°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도the temperature was increased to between 35° C. and 40° C
  2. 2
    workup.WAITThe reaction mixture was placed under vacuum for 10 minutes
  3. 3
    기타to remove the chlorotrimethylsilane (b.p.=57° C.)
  4. 4
    workup.WAITAfter 10 minutes
  5. 5
    온도After cooling
  6. 6
    workup.ADDITIONthe reaction mixture was poured into water (1.2 L)
  7. 7
    추출extracted with ether (3×)
  8. 8
    세척The combined organic layers were washed with water (3×) and brine
  9. 9
    기타dried
  10. 10
    농축concentrated

실험 절차

To a solution of 4-(chlorocarbonyl)phenyl acetate (45.6 g, 0.23 mol) in sulfolane (200 mL) was added 2-TMS-1,2,3-triazole (1.1 eq., 34 mL) over one minute. After stirring for 5 minutes under nitrogen, the reaction was exothermic and the temperature was increased to between 35° C. and 40° C. The reaction mixture was placed under vacuum for 10 minutes to remove the chlorotrimethylsilane (b.p.=57° C.). The reaction mixture was heated at 150° C. for 2.5 hours. After 10 minutes, gas evolution was observed. After cooling, the reaction mixture was poured into water (1.2 L) and extracted with ether (3×). The combined organic layers were washed with water (3×) and brine, dried and concentrated to give 4-(2-oxazolyl)phenyl acetate (44.8 g, 96% th.; 98% pract) as a solid; 1H NMR (CDCl3) δ 8.05 (d, 2H), 7.70 (s, 1H), 7.20 (m, 3H), 2.35 (s, 3H) ppm.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07737145B2uspto-grants-2010_06