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Ethylene Glycol → 4-{[4-(1,3-Dioxolan-2-yl)-2-(methyloxy)phenyl]oxy}-2-nitroaniline

HRID 547627
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HRID 547627 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]2[CH:16]=[CH:15][C:12]([CH:13]=[O:14])=[CH:11][C:10]=2[O:17][CH3:18])=[CH:4][C:3]=1[N+:19]([O-:21])=[O:20].[CH2:22](O)[CH2:23][OH:24].C1(C)C=CC(S(O)(=O)=O)=CC=1>C1(C)C=CC=CC=1.C(OCC)(=O)C>[O:14]1[CH2:22][CH2:23][O:24][CH:13]1[C:12]1[CH:15]=[CH:16][C:9]([O:8][C:5]2[CH:6]=[CH:7][C:2]([NH2:1])=[C:3]([N+:19]([O-:21])=[O:20])[CH:4]=2)=[C:10]([O:17][CH3:18])[CH:11]=1
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참가 물질

6

반응물 3

HCID 174Ethylene GlycolHCID 6101p-Toluenesulfonic acidHCID 575858814-[(4-Amino-3-nitrophenyl)oxy]-3-(methyloxy)benzaldehyde

생성물 1

HCID 575859654-{[4-(1,3-Dioxolan-2-yl)-2-(methyloxy)phenyl]oxy}-2-nitroaniline

시약·촉매·용매 2

HCID 1140Toluene용매HCID 8857
Ethyl Acetate
용매

실험 절차

4-[(4-amino-3-nitrophenyl)oxy]-3-(methyloxy)benzaldehyde (2.42 g, 8.4 mmol), ethyleneglycol (4 ml) and p-toluenesulfonic acid (50 mg) in 50 mL of toluene was heated at 125 degrees Centigrade with a Dean-Stark trap for approximately 18 hours. The reaction mixture was diluted with ethyl acetate and washed twice with saturated NaHCO3. The aqueous layers were extracted with ethyl acetate. The organic layers were combined, dried over MgSO4 and concentrated to give 4-{[4-(1,3-dioxolan-2-yl)-2-(methyloxy) phenyl]oxy}-2-nitroaniline. (M+1) 332.9, 2.13 min (LC/MS method B)

후처리

  1. washwashed twice with saturated NaHCO3
  2. extractionThe aqueous layers were extracted with ethyl acetate
  3. dry with materialdried over MgSO4
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-734c4a7a7a9a432ca7bdeb577a62e350
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07939528B2

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