2-Methylbenzenesulfonic acid → HCID 22768127、化合物

HRID 1764415ノート

反応式

HRID 1764415 の反応式
[CH:1]([N:4]([CH2:9][CH:10]([O:14]CC)[O:11][CH2:12]C)[C:5](=[O:8])[CH2:6][Cl:7])([CH3:3])[CH3:2].[C:17]1([CH3:27])[C:18](S(O)(=O)=O)=CC=C[CH:22]=1.C(=O)([O-])[O-].[Na+].[Na+]>C(O)C>[CH:1]([N:4]([CH2:9][CH:10]1[O:14][CH2:22][C:17]([CH3:18])([CH3:27])[CH2:12][O:11]1)[C:5](=[O:8])[CH2:6][Cl:7])([CH3:3])[CH3:2]

参加物

5

実験手順

N-Isopropyl-N-(2,2-diethoxyethyl)-α-chloroacetamide (10 grams), 2,2-dimethylpropandiol-1,3 (4.1 grams) 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 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-(5,5-dimethyl-1,3-dioxan-2-ylmethyl)-α-chloroacetamide having a boiling point of 175° 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. distillationthe resulting mixture was distilled

出典と根拠

ORDレコード
ord-94a5ad17770a463c9e31ecf3e4b2b2ef
出典データセット
uspto-grants-1978_09
特許番号
US04116670

反応ノート

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