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

HRID 1446958

Reaktionsgleichung

Reaktionsgleichung von HRID 1446958
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

Komponenten

5

Reaktionsbedingungen

Temperatur
110 °C

Versuchsvorschrift

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.

Aufarbeitung

  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

Quellen und Nachweise

ORD-Eintrag
ord-df5f30e24d8848b2aa8a27dab98251d0
Quelldatensatz
uspto-grants-1982_02
Patentnummer
US04314840

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