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Water → 3-Ethoxy-4-nitrobenzaldehyde

HRID 856743
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HRID 856743 반응식
[OH:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[N+:10]([O-:12])=[O:11])[CH:5]=[O:6].C(=O)([O-])[O-].[K+].[K+].I[CH2:20][CH3:21].O>CN(C=O)C>[CH2:20]([O:1][C:2]1[CH:3]=[C:4]([CH:7]=[CH:8][C:9]=1[N+:10]([O-:12])=[O:11])[CH:5]=[O:6])[CH3:21]
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참가 물질

6

반응물 4

HCID 962WaterHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 697123-Hydroxy-4-nitrobenzaldehyde

생성물 1

HCID 220388973-Ethoxy-4-nitrobenzaldehyde수율 69.7%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a suspension of 3-hydroxy-4-nitrobenzaldehyde (7.0 g) and potassium carbonate (8.1 g) in DMF (100 ml), iodoethane (8.3 g) was added dropwise under nitrogen atmosphere. The mixture was stirred overnight, water was added to the mixture and the mixture was extracted with ethyl acetate. The organic layer was washed with water once and saturated brine once, and dried over magnesium sulfate. The solvent was distilled off under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=0.1:1), and recrystallized from hexane-ethyl acetate, to give 3-ethoxy-4-nitrobenzaldehyde (5.7 g) as yellow crystals.

후처리

  1. additionwas added dropwise under nitrogen atmosphere
  2. extractionthe mixture was extracted with ethyl acetate
  3. washThe organic layer was washed with water once
  4. dry with materialsaturated brine once, and dried over magnesium sulfate
  5. distillationThe solvent was distilled off under reduced pressure
  6. customthe obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=0.1:1)
  7. customrecrystallized from hexane-ethyl acetate

출처 및 근거

ORD 기록
ord-5cf460cb618947b9ba8ecd80bacd2522
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262185B2

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