반응 #685036

ord-f5f0420a82aa48078fc28410384ae386

반응 방정식

O=C([O-])O.[Na+]
sodium bicarbonate
O=S(=O)(Cl)Cl
sulfuryl chloride
CC(=O)c1ccc(Cl)cc1F
4′-chloro-2′-fluoroacetophenone
CO
methanol
O=C(CCl)c1ccc(Cl)cc1F
2-Chloro-1-(4-chloro-2-fluorophenyl)ethanone

반응 조건

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

후처리

  1. 1
    기타In a 1 L round bottom flask combine
  2. 2
    workup.ADDITIONAdd
  3. 3
    기타drop-wise to the reaction over 60 min
  4. 4
    workup.ADDITIONthen add to the reaction drop-wise
  5. 5
    여과filter the biphasic suspension
  6. 6
    기타to collect the title compound (38.18 g, 80%) as white needles

실험 절차

In a 1 L round bottom flask combine 4′-chloro-2′-fluoroacetophenone (40 g, 231.8 mmol), heptane (120 mL), and methanol (16 mL). Cool to 0° C. and place under nitrogen. Dissolve sulfuryl chloride (21.5 mL, 1.15 equiv.) in heptane (120 mL) and charge to an addition funnel Add drop-wise to the reaction over 60 min. Stir for 2.5 h at 0° C.; a white precipitate forms during this time. Charge the addition funnel with 1 M sodium bicarbonate (400 mL) then add to the reaction drop-wise. After all gas evolution stops, filter the biphasic suspension to collect the title compound (38.18 g, 80%) as white needles. 1H NMR (DMSO-d6) δ 5.00 (d, 2H, J=2.5 Hz), 7.43 (m, 1H), 7.63 (m, 1H), 7.89 (t, 1H, J=8.4 Hz).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07897600B2uspto-grants-2011_03