Sodium Hydroxide → 2-Butyl-5-chloro-1H-imidazole-4-carbaldehyde

HRID 375691노트

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HRID 375691 반응식
[CH2:1]([C:5]1[NH:6][C:7](=O)[C:8](=[CH:10]N(C)C)[N:9]=1)[CH2:2][CH2:3][CH3:4].O=P(Cl)(Cl)[Cl:17].[OH-:20].[Na+]>O>[CH2:1]([C:5]1[NH:6][C:7]([Cl:17])=[C:8]([CH:10]=[O:20])[N:9]=1)[CH2:2][CH2:3][CH3:4]

참가 물질

5

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온도
100 °C

실험 절차

A mixture of 1.00 g (5.12 mmol) of 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one and 3.20 g (20.48 mmol) of POCl3 was heated at 100° C. for 45 minutes. Then, 1.76 g of POCl3 was distilled off on the Rotavapor, and the residue was treated with 6 ml of ethyl acetate. The mixture thus obtained was added to 20 ml of water, and the water was stirred at room temperature for 5 minutes. Then, the pH was adjusted from 0.34 to 7, using 30 percent strength sodium hydroxide solution. The mixture was extracted twice, using 10 ml of ethyl acetate each time. The combined organic phases were dried (MgSO4), filtered and concentrated, and the residue was dried in a high vacuum. 0.89 g of 2-butyl-5-chloroimidazole-4-carbaldehyde was obtained; this product having a purity greater than 95 percent, according to H-NMR. This corresponds to a yield of 93 percent, based on the 2-butyl-4-dimethylaminomethylene-2-imidazolin-5-one.

후처리

  1. distillationThen, 1.76 g of POCl3 was distilled off on the Rotavapor
  2. additionthe residue was treated with 6 ml of ethyl acetate
  3. customThe mixture thus obtained
  4. extractionThe mixture was extracted twice
  5. dry with materialThe combined organic phases were dried (MgSO4)
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe residue was dried in a high vacuum

출처 및 근거

ORD 기록
ord-9e60c15d2bd143bebd915a52c9bc8cd0
출처 데이터셋
uspto-grants-1996_01
특허 번호
US05486617

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