HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1732210Generated: October 25, 2026
Ethylene Glycol → N-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide
https://huagongshe.com/reaction/1732210
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethylene Glycol | HCID 174 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamide | HCID 12850700 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamide | HCID 12850701 | — |
Reaction Steps
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.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04237056 |
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| Source dataset | uspto-grants-1980_12 |
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| ORD ID | ord-f90b6eb7cd2f47f1a8856b596b57a3ce |
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| Source note | uspto-grants-1980_12 |
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