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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1763761Generated: November 2, 2026

Diethyl Ether → 2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamide

https://huagongshe.com/reaction/1763761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantChloroacetyl chlorideHCID 6577—
ReactantTriethylamineHCID 8471—
Reactant2-(Methylamino)acetaldehydeHCID 13316132—
SolventDichloromethaneHCID 6344—
Product2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamideHCID 12850700—

Reaction Conditions

Temperature-20 °C

Reaction Steps

The dimethylacetal of 2-methylaminoacetaldehyde (50 grams; 0.42 mole), methylene chloride (200 ml) and triethylamine (46.6 grams; 0.462 mole) were charged into a glass reaction vessel equipped with a mechanical stirrer, thermometer, addition funnel and calcium chloride drying tube. The reaction mixture was cooled to about -20° C. and chloroacetyl chloride (49.7 grams; 0.44 mole) dissolved in methylene chloride (29 ml) was added dropwise with stirring. After the addition was completed stirring was continued for a period of about 60 minutes at a temperature of from -20° C. to -10° C. The reaction mixture was then stirred at room temperature overnight. After this time ether (125 ml) was added and the reaction mixture was filtered. The filtrate was then washed with water and dilute aqueous sodium hydroxide. The washed solution was dried over anhydrous magnesium sulfate, filtered and stripped of solvent under reduced pressure to yield the desired product N-methyl-N-(2,2-dimethoxyethyl)-α-chloroacetamide having a boiling point of 117° to 119° C. at 0.30 mm of Hg pressure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04113464
Source datasetuspto-grants-1978_09
ORD IDord-aa57b0fed9a2463a99562e27e054faee
Source noteuspto-grants-1978_09