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Dimethylformamide → 1-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde

HRID 2427093
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HRID 2427093 반응식
P(Cl)(Cl)(Cl)=O.[Cl:6][C:7]1[C:12]([N:13]2[CH:17]=[CH:16][CH:15]=[CH:14]2)=[CH:11][CH:10]=[CH:9][N:8]=1.[OH-].[Na+].CN(C)[CH:22]=[O:23]>>[Cl:6][C:7]1[C:12]([N:13]2[CH:17]=[CH:16][CH:15]=[C:14]2[CH:22]=[O:23])=[CH:11][CH:10]=[CH:9][N:8]=1
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참가 물질

5

반응물 4

HCID 6228DimethylformamideHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 27579082-chloro-3-(1H-pyrrol-1-yl)pyridine

생성물 1

HCID 27723241-(2-Chloro-pyridin-3-yl)-1H-pyrrole-2-carbaldehyde수율 80.5%

실험 절차

To 14.6 g of N,N-dimethylformamide was added dropwise 8.3 g of phosphorus oxychloride under ice-cooling. The mixture was stirred at room temperature for 30 minutes. Thereto 6.5 g of 1-(2-chloro-3-pyridinyl)-1H-pyrrole was added, and the resulting mixture was stirred at 60° C. for 2 hours. The reaction mixture was allowed to cool to room temperature, and added to ice water. The mixture was adjusted to pH 4 by an addition of a 2N aqueous sodium hydroxide solution, and then extracted with ethyl acetate two times. The organic layers were combined, washed successively with water and an aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The resulting residue was subjected to silica gel chromatography to obtain 6.05 g of 1-(2-chloro-3-pyridinyl)-1H-pyrrole-2-carbaldehyde of the formula:

후처리

  1. temperaturecooling
  2. stirringthe resulting mixture was stirred at 60° C. for 2 hours
  3. temperatureto cool to room temperature
  4. extractionextracted with ethyl acetate two times
  5. washwashed successively with water
  6. dry with materialan aqueous saturated sodium chloride solution, dried over anhydrous sodium sulfate
  7. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-db45241e5dec408989ce0cd141d32c04
출처 데이터셋
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07968573B2

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