2-Methylbenzenesulfonic acid → HCID 20307412, 화합물

HRID 1763773노트

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HRID 1763773 반응식
[CH:1]([N:4]([CH2:9][CH:10]([O:14][CH2:15][CH3:16])[O:11][CH2:12]C)[C:5](=[O:8])[CH2:6][Cl:7])([CH3:3])[CH3:2].[C:17]1(C)C(S(O)(=O)=O)=CC=CC=1.C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[CH:1]([N:4]([CH2:9][CH:10]1[O:14][CH:15]([CH2:16][CH3:17])[CH2:12][O:11]1)[C:5](=[O:8])[CH2:6][Cl:7])([CH3:2])[CH3:3]

참가 물질

5

실험 절차

N-Isopropyl-N-(2,2-diethoxyethyl)-α-chloroacetamide (10 grams), butandiol-1,2 (3.56 ml) and trace amounts of toluenesulfonic acid were charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer and reflux condenser. The reaction mixture was heated at reflux until no more ethanol was given off. After this time sodium carbonate (1 gram) was added to the mixture with stirring and the resulting mixture was distilled to yield the desired product N-isopropyl-N-(4-ethyl-1,3-dioxolan-2-ylmethyl)-α-chloroacetamide having a boiling point of 140° C. at 1 mm of Hg pressure.

후처리

  1. additionwere charged into a glass reaction vessel
  2. customequipped with a mechanical stirrer
  3. temperaturethermometer and reflux condenser
  4. temperatureThe reaction mixture was heated
  5. distillationthe resulting mixture was distilled

출처 및 근거

ORD 기록
ord-a1e2858dd1af4f069ecfb92f2814e090
출처 데이터셋
uspto-grants-1978_09
특허 번호
US04113464

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