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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1446955Erstellt: 25. Oktober 2026

Ethylene Glycol → N-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide

https://huagongshe.com/reaction/1446955

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthylene GlycolHCID 174—
Eduktp-Toluenesulfonic acidHCID 6101—
Edukt2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamideHCID 12850700—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamideHCID 12850701—

Reaktionsschritte

N-Methyl-N-(2,2-dimethoxyethyl)-2-chloroacetamide (19.5 grams; 0.10 mole), ethylene glycol (6.82 grams; 0.11 mole) and 10 drops of a solution of one gram of p-toluenesulfonic acid in 100 ml of diethyl ether were charged into a glass reaction vessel fitted with a mechanical stirrer, thermometer, distillation head and condenser. The mixture was stirred and heated to about 100° C. to 110° C. Byproduct methanol was distilled off. When no further methanol was evolved, the mixture was cooled to room temperature, sodium carbonate (2 grams) was added and the slurry was stirred for a period of about 1 hour. The slurry was then filtered and the filtrate fractionally distilled under reduced pressure. The desired product N-(1,3-dioxolan-2-ylmethyl)-N-methyl-2-chloroacetamide was obtained as a fraction boiling at 124° C. at 0.30 mm Hg and at 119° C. at 0.15 mm Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04314840
Quelldatensatzuspto-grants-1982_02
ORD IDord-cd003996d60b47a686229db101df259f
Quellennotizuspto-grants-1982_02