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Glycerol → 7-Methyl-6-nitroquinoline

HRID 1991062
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인쇄 미리보기

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HRID 1991062 반응식
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([N+:11]([O-:13])=[O:12])=[C:7]([CH3:14])[CH:6]=1)(=O)[CH3:2].O[CH2:16]C(CO)O.OS(O)(=O)=O>>[CH3:14][C:7]1[CH:6]=[C:5]2[C:10]([CH:16]=[CH:2][CH:1]=[N:4]2)=[CH:9][C:8]=1[N+:11]([O-:13])=[O:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 753GlycerolHCID 1118Sulfuric AcidHCID 27373784-Acetamido-2-methylnitrobenzene

생성물 1

HCID 36408347-Methyl-6-nitroquinoline수율 34.4%

실험 절차

4-Acetamido-2-methylnitrobenzene (4.5 g; 23.2 mmol) glycerol (9 g; 100 mmol), H2SO4 conc (6.75 g) and As2O5.5H2O (3.6 g; 46.4 mmol) were heated at 130° C. for 20 h. The reaction mixture was poured on water, adjusted to pH 7-8 by adding NH3conc. and extracted with EtOAc three times. The combined organic phases were dried over Na2SO4, evaporated and purified via chromatography (SiO2; TBME/hexanes 70/30) to yield the title compound (1.5 g; 34%). The isomeric 5-methyl-6-nitroquinoline was eluted from the column after the title compound (850 mg; 19%).

후처리

  1. additionThe reaction mixture was poured on water
  2. additionby adding NH3conc
  3. extractionand extracted with EtOAc three times
  4. dry with materialThe combined organic phases were dried over Na2SO4
  5. customevaporated
  6. custompurified via chromatography (SiO2; TBME/hexanes 70/30)

출처 및 근거

ORD 기록
ord-50eb3d652f894a71a2efe09055562c23
출처 데이터셋
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07645760B2

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