2-Methoxyethanol → 2-Chloro-6-(2-methoxyethoxy)-4-(trichloromethyl)pyridine

HRID 614077

반응식

HRID 614077 반응식
Cl[C:2]1[CH:7]=[C:6]([C:8]([Cl:11])([Cl:10])[Cl:9])[CH:5]=[C:4]([Cl:12])[N:3]=1.[Na].[CH3:14][O:15][CH2:16][CH2:17][OH:18]>>[Cl:12][C:4]1[CH:5]=[C:6]([C:8]([Cl:11])([Cl:10])[Cl:9])[CH:7]=[C:2]([O:18][CH2:17][CH2:16][O:15][CH3:14])[N:3]=1

참가 물질

4

실험 절차

To a solution of 26.54 grams (0.10 mole) of 2,6-dichloro-4-(trichloromethyl)pyridine dissolved in 150 milliliters (ml) of 2-methoxyethanol was added over a 35 minute period, a solution composed of 2.53 grams (0.11 mole) of sodium metal dissolved in 100 ml of 2-methoxyethanol. The mixture was stirred for 5 hours at 65°-75° C. The insoluble by-products were removed by filtration and the 2-methoxyethanol was removed by evaporation under reduced pressure. The resulting oily product was diluted with water and extracted with methylene chloride and dried with sodium sulfate. The methylene chloride was then removed leaving the 2-chloro-6-(2-methoxyethoxy)-4-(trichloromethyl)pyridine as an oil. The product was recovered in a yield of 25.6 grams (84 percent of theoretical) and had a refractive index of n 25/d = 1.5440. Upon analysis, the compound was found to have carbon, hydrogen and nitrogen contents of 35.48, 2.99 and 4.72 percent, respectively, as compared with the theoretical contents of 35.44, 2.97 and 4.59 percent, respectively, as calculated for the above named structure.

후처리

  1. additionwas added over a 35 minute period
  2. customThe insoluble by-products were removed by filtration
  3. customthe 2-methoxyethanol was removed by evaporation under reduced pressure
  4. additionThe resulting oily product was diluted with water
  5. extractionextracted with methylene chloride
  6. dry with materialdried with sodium sulfate
  7. customThe methylene chloride was then removed

출처 및 근거

ORD 기록
ord-b0b65b64916149bea499c561a78da65e
출처 데이터셋
uspto-grants-1979_03
특허 번호
US04143144

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