Sulfuric Acid → 1-Bromo-2,5-dichloro-3-nitrobenzene

HRID 429139

반응식

HRID 429139 반응식
S(=O)(=O)(O)O.[Br:6][C:7]1[C:13]([Cl:14])=[C:12]([N+:15]([O-:17])=[O:16])[C:11](Cl)=[CH:10][C:8]=1N.N([O-])=O.[Na+].[Cl:23]CCl>C(O)C.C(=O)([O-])O.[Na+]>[Br:6][C:7]1[C:13]([Cl:14])=[C:12]([N+:15]([O-:17])=[O:16])[CH:11]=[C:10]([Cl:23])[CH:8]=1

참가 물질

7

반응물 4

HCID 1118Sulfuric AcidHCID 6344DichloromethaneHCID 183545642-Bromo-3,5-dichloro-4-nitroanilineHCID 23668193Sodium Nitrite

생성물 1

HCID 183545541-Bromo-2,5-dichloro-3-nitrobenzene수율 80%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 516892Sodium Bicarbonate용매

실험 절차

Concentrated sulphuric acid (2.2 ml) was slowly added to a suspension of 2-bromo-3,5-dichloro-4-nitroaniline (D8) (0.9 g, 3.1 mmol) in ethanol (20 ml). The resulting solution was heated to reflux and crushed sodium nitrite (478 mg, 6.9 mmol) was added in two portions. After 0.5 h at reflux, the mixture was cooled, diluted with dichloromethane (50 ml) and saturated sodium hydrogen carbonate solution (50 ml) was added. The layers were separated and the organic phase dried (Na2SO4) and concentrated to an oil which was purified by column chromatography over silica gel eluting with a gradient of ethyl acetate/hexane to give the title compound (D9) as an orange solid (0.67 g, 80%), MH+ 269/271.

후처리

  1. temperatureThe resulting solution was heated
  2. temperatureto reflux
  3. additionwas added in two portions
  4. temperatureAfter 0.5 h at reflux
  5. temperaturethe mixture was cooled
  6. additionwas added
  7. customThe layers were separated
  8. dry with materialthe organic phase dried (Na2SO4)
  9. concentrationconcentrated to an oil which
  10. customwas purified by column chromatography over silica gel eluting with a gradient of ethyl acetate/hexane

출처 및 근거

ORD 기록
ord-f3d99b8097e947bf84a8f0afd32323f5
출처 데이터셋
uspto-grants-2001_11
특허 번호
US06316450B1

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