2-Methylbenzenesulfonic acid → HCID 20307412、化合物

HRID 1763773ノート

反応式

HRID 1763773 の反応式
[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]

参加物

5

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-a1e2858dd1af4f069ecfb92f2814e090
出典データセット
uspto-grants-1978_09
特許番号
US04113464

反応ノート

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