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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamideHCID 12850700—
SolventDiethyl EtherHCID 3283—
ProductN-methyl-N-(1,3-dioxolan-2-ylmethyl)-alpha-chloroacetamideHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04237056
Source datasetuspto-grants-1980_12
ORD IDord-f90b6eb7cd2f47f1a8856b596b57a3ce
Source noteuspto-grants-1980_12