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Sulfuric Acid → 6-Bromo-8-methylquinoline

HRID 655234
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HRID 655234 반응식
[Br:1][C:2]1[CH:8]=[CH:7][C:5]([NH2:6])=[C:4]([CH3:9])[CH:3]=1.[N+]([C:13]1[CH:18]=CC=C[CH:14]=1)([O-])=O.S(=O)(=O)(O)O>OCC(CO)O>[Br:1][C:2]1[CH:8]=[C:7]2[C:5](=[C:4]([CH3:9])[CH:3]=1)[N:6]=[CH:18][CH:13]=[CH:14]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1118Sulfuric AcidHCID 7416NitrobenzeneHCID 114234-Bromo-2-methylaniline

생성물 1

HCID 224034106-Bromo-8-methylquinoline

시약·촉매·용매 1

HCID 753Glycerol용매

실험 절차

A mixture of 10 g of 4-bromo-2-methylaniline, 3.3 g of ferrous sulfate, 20.4 g of glycerol, 4.06 g of nitrobenzene and 11.5 ml of concentrated sulfuric acid was heated gently. After the first vigorous reaction, the mixture was boiled for 3 h under reflux and then evaporated to remove t nitrobenzene. The solution was added std. aq.NaHCO3 and extracted with dichloromethane, dried with Na2SO4 and concentrated to give solid. The solid was purified with flash column chromatography to return the title compound (9.5 g, 80%). 1H NMR (CDCl3, 300 MHz) δ 8.92 (m, 1H), 8.01 (m, 1H), 7.81 (d, 1H), 7.66 (m, 1H), 7.43 (m, 1H), 2.79 (s, 3H).

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후처리

  1. temperaturewas heated gently
  2. customAfter the first vigorous reaction
  3. temperatureunder reflux
  4. customevaporated
  5. customto remove t nitrobenzene
  6. additionThe solution was added std
  7. extractionNaHCO3 and extracted with dichloromethane
  8. dry with materialdried with Na2SO4
  9. concentrationconcentrated
  10. customto give solid
  11. customThe solid was purified with flash column chromatography

출처 및 근거

ORD 기록
ord-227e052f4b254e398841384dca6709fb
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071581B2

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