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Dimethylformamide → HCID 22494013, 화합물

HRID 1816656
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HRID 1816656 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4](O)[CH:3]=1.[CH2:12](I)[CH3:13].[C:15](=O)([O-])[O-].[K+].[K+].CN(C)[CH:23]=[O:24]>O>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:8][CH2:12][CH3:13])=[O:7])=[C:4]([O:24][CH2:23][CH3:15])[CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6228DimethylformamideHCID 6340IodoethaneHCID 11430Potassium CarbonateHCID 787824-Chlorosalicylic acid

생성물 1

HCID 22494013HCID 22494013, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
70 °C

실험 절차

5.0 g of 4-chloro-2-hydroxybenzoic acid was dissolved in 25 ml dimethylformamide, and 14.5 g of ethyl iodide and 12 g of potassium carbonate were added thereto, followed by stirring at 70° C. for 8 hours. The reaction solution was diluted with water and then extracted with ethyl acetate. The organic layer was successively washed with 1N hydrochloric acid and brine, dried over anhydrous magnesium sulfate and the solvent was evaporated. The residue was subjected to silica gel column chromatography, and from fractions eluted with hexane-ethyl acetate (2:1), 3.8 g of ethyl 4-chloro-2-ethoxybenzoate was obtained.

후처리

  1. extractionextracted with ethyl acetate
  2. washThe organic layer was successively washed with 1N hydrochloric acid and brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customthe solvent was evaporated
  5. washfrom fractions eluted with hexane-ethyl acetate (2:1)

출처 및 근거

ORD 기록
ord-13672613756e4ca7a67eedb6eda20735
출처 데이터셋
uspto-grants-2005_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06884821B1

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