반응 #309648

ord-94d359c972a44d06b9dbdeb5dffb2e22

반응 조건

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

후처리

  1. 1
    온도while maintaining the temperature at 0-5° C
  2. 2
    여과the mixture was filtered through a cotton pad
  3. 3
    workup.WAITAfter standing overnight
  4. 4
    세척washed with 10% aq NaOH and 5% aq Na2S2O5 successively
  5. 5
    건조dried over MgSO4
  6. 6
    여과filtered
  7. 7
    농축concentrated
  8. 8
    기타The residue was purified by column chromatography (ethyl acetate:hexane; 2:98)

실험 절차

2-Fluoro-4-methyl-5-nitro-aniline (1.30 g, 7.64 mmol) was suspended in concentrated hydrochloric acid (4 mL) and cooled to 0° C. Solution of sodium nitrite (0.58 g, 8.40 mmol) in water (2.6 mL) was added dropwise while maintaining the temperature at 0-5° C. After stirring for 15 min, the mixture was filtered through a cotton pad and slowly poured into a solution of potassium iodide (4.44 g, 26.7 mmol) in water (16 mL). After standing overnight, the reaction mixture was diluted with EtOAc, washed with 10% aq NaOH and 5% aq Na2S2O5 successively, dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography (ethyl acetate:hexane; 2:98) to afford 1-iodo-2-fluoro-4-methyl-5-nitro-benzene as a colorless oil (1.60 g, 74%). 1H NMR (CDCl3, 400 MHz,): 2.61 (s, 3H), 7.05 (d, J=8.0 Hz, 1H), 8.44 (d, J=5.8 Hz, 1H). 13C NMR (CDCl3, 100 MHz,): 20.7, 119.1, 136.2, 137.3, 145.7, 163.9.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08207216B2uspto-grants-2012_06