4-Chloro-2,3,5-trimethyl-1-oxidopyridin-1-ium → HCID 24816049, 화합물

HRID 31723

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HRID 31723 반응식
Cl[C:2]1[C:7]([CH3:8])=[CH:6][N+:5]([O-:9])=[C:4]([CH3:10])[C:3]=1[CH3:11].[CH3:12][C:13]1([CH3:21])[O:18][CH2:17][CH:16]([CH2:19][OH:20])[CH2:15][O:14]1>C1(C)C=CC=CC=1>[CH3:12][C:13]1([CH3:21])[O:18][CH2:17][CH:16]([CH2:19][O:20][C:2]2[C:7]([CH3:8])=[CH:6][N+:5]([O-:9])=[C:4]([CH3:10])[C:3]=2[CH3:11])[CH2:15][O:14]1

참가 물질

4

실험 절차

A mixture of 4-chloro-2,3,5-trimethylpyridine 1-oxide (840 g), (2,2-dimethyl-1,3-dioxan-5-yl)methanol (688 g) and toluene (2.52 L) was heated under reflux while removing a water content. While azeotropical dehydration was continued, potassium hydroxide (0.58 kg) was added to the reaction mixture over 3 hours and 45 minutes, and azeotropic dehydration was continued for 2.5 hours. The mixture was cooled to 30° C. or less, and ethyl acetate (2.5 L) and a 17% saline solution (3.5 L) were added to the mixture and then the mixture was allowed to stand for overnight. The ethyl acetate layer was separated and the aqueous layer was extracted with ethyl acetate (1.0 L×3). The ethyl acetate layers were combined, filtrated through celite, and concentrated under reduced pressure to obtain a desired product (1.20 kg).

후처리

  1. temperaturewas heated
  2. temperatureunder reflux
  3. customwhile removing a water content
  4. additionpotassium hydroxide (0.58 kg) was added to the reaction mixture over 3 hours and 45 minutes
  5. temperatureThe mixture was cooled to 30° C. or less
  6. additionethyl acetate (2.5 L) and a 17% saline solution (3.5 L) were added to the mixture
  7. waitto stand for overnight
  8. customThe ethyl acetate layer was separated
  9. extractionthe aqueous layer was extracted with ethyl acetate (1.0 L×3)
  10. filtrationfiltrated through celite
  11. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-54dbbcbe5d074cb09cd083371b18cc7c
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07425634B2

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