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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethylene Glycol | HCID 174 | — |
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamide | HCID 12850700 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | N-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04314840 |
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| Quelldatensatz | uspto-grants-1982_02 |
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| ORD ID | ord-cd003996d60b47a686229db101df259f |
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| Quellennotiz | uspto-grants-1982_02 |
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