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Glycerol → 5-Methyl-8-nitroquinoline

HRID 513385
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인쇄 미리보기

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HRID 513385 반응식
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:9]([O-:11])=[O:10])=[C:6]([CH:8]=1)[NH2:7].O[CH2:13][CH:14]([CH2:16]O)O.[Na+].[N+](C1C=C(S([O-])(=O)=O)C=CC=1)([O-])=O.OS(O)(=O)=O.O>>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]([N+:9]([O-:11])=[O:10])=[C:6]2[C:8]=1[CH:13]=[CH:14][CH:16]=[N:7]2
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참가 물질

5

반응물 4

HCID 753GlycerolHCID 113566-Nitro-m-toluidineHCID 31389Sodium 3-nitrobenzenesulfonateHCID 21910475Sulfuric acid hydrate (1:1)

생성물 1

HCID 64278395-Methyl-8-nitroquinoline수율 77%

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온도
105 °C

실험 절차

5-methyl-2-nitroaniline (1.0 g, 6.57 mmol), glycerol (1.88 g, 20.4 mmol), 3-nitrobenzenesulfonic acid sodium salt (1.92 g, 8.54 mmol) were added to H2SO4/H2O (6 ml, 7:5) solution and heated at 105° C. for 48 h. After completion of the reaction (monitored by LCMS), the mixture was cooled to 45° C. and poured slowly onto ice water (50 ml) and the mixture was extracted with DCM. The combined organic phases were dried (Na2SO4) and concentrated in vacuo to give the title compound (950 mg, 77%) which was used in the next step without purification.

후처리

  1. customAfter completion of the reaction (monitored by LCMS)
  2. temperaturethe mixture was cooled to 45° C.
  3. additionpoured slowly onto ice water (50 ml)
  4. extractionthe mixture was extracted with DCM
  5. dry with materialThe combined organic phases were dried (Na2SO4)
  6. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-1cd3903bd707449d9bc84035a949d405
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09102688B2

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