반응 #607399

ord-63fc97e5fd3d44d39a240323a87e0b52

반응 방정식

O=[N+]([O-])c1ccc(-c2ncn(-c3ccc(C(F)(F)F)cc3)n2)cc1
3-(4-nitrophenyl)-1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazole
Nc1ccc(-c2ncn(-c3ccc(C(F)(F)F)cc3)n2)cc1
title compound
수율 77.9%
Nc1ccc(-c2ncn(-c3ccc(C(F)(F)F)cc3)n2)cc1
4-(1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazol-3-yl)aniline
수율 77.9%

반응 조건

온도
90°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction was cooled to room temperature
  2. 2
    여과filtered through Celite®
  3. 3
    세척wash
  4. 4
    기타The organic layer was separated
  5. 5
    농축concentrated
  6. 6
    기타Purification by flash column chromatography

실험 절차

To 3-(4-nitrophenyl)-1-(4-(trifluoromethyl)phenyl)-1H-1,2,4-triazole (22.0 g, 65.8 mmol) in acetic acid (132 mL) and water (110 mL) was added iron powder. The reaction was heated to 90° C. for 18 hours. The reaction was cooled to room temperature and filtered through Celite® followed by an ethyl acetate wash. The organic layer was separated and concentrated. Purification by flash column chromatography using 0-50% ethyl acetate/petroleum ether as eluent provided the title compound as a light yellow solid (15.6 g, 74%): 1H NMR (300 MHz, CDCl3) δ 8.00 (d, J=1.0 Hz, 1H), 7.68-6.92 (m, 6H), 6.29-5.93 (m, 2H), 3.27 (bs, 2H); ESIMS m/z 305 ([M+H]+).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09326516B2uspto-grants-2016_05