2,3-Butanediol → N-(4,5-Dimethyl-1,3-dioxolan-2-YL)-N-methyl-2-chloroacetamide

HRID 1446958

反応式

HRID 1446958 の反応式
COC(OC)[CH2:4][N:5]([CH3:10])[C:6](=[O:9])[CH2:7][Cl:8].[CH3:13][CH:14]([OH:18])[CH:15]([OH:17])[CH3:16].C1(C)C=CC(S(O)(=O)=O)=CC=1>CO>[CH3:16][CH:15]1[CH:14]([CH3:13])[O:18][CH:4]([N:5]([CH3:10])[C:6](=[O:9])[CH2:7][Cl:8])[O:17]1

参加物

5

反応条件

温度
110 °C

実験手順

N-(2,2-Dimethoxyethyl)-N-methyl-2-chloroacetamide (97.8 grams; 0.5 mole), 2,3-butanediol (45 grams) and 0.2 grams p-toluenesulfonic acid were charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, distilling head and condenser. The reaction mixture was heated at about 90° C. to 100° for a period of 5 hours. Little reaction occurred as shown by the absence of methanol distilled. The reaction mixture was then heated at about 110° C., for about 2 hours at atmospheric pressure, then 1 hour at reduced pressure. Under these more rigorous conditions, methanol was formed and was distilled off. At the conclusion of the reaction, the reaction mixture was distilled and the fraction boiling at 127° C. to 130° C. at 0.55 mm Hg was the desired product N-(4,5-dimethyl-1,3-dioxolan-2-yl)-N-methyl-2-chloroacetamide.

後処理

  1. customfitted with a mechanical stirrer
  2. distillationthermometer, distilling head and condenser
  3. temperatureThe reaction mixture was heated at about 90° C. to 100° for a period of 5 hours
  4. customLittle reaction
  5. distillationdistilled
  6. custom1 hour
  7. customUnder these more rigorous conditions, methanol was formed
  8. distillationwas distilled off
  9. customAt the conclusion of the reaction
  10. distillationthe reaction mixture was distilled

出典と根拠

ORDレコード
ord-df5f30e24d8848b2aa8a27dab98251d0
出典データセット
uspto-grants-1982_02
特許番号
US04314840

関連ノート

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