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HRID 1446954Erstellt: 25. Oktober 2026

Chloroacetyl chloride → 2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamide

https://huagongshe.com/reaction/1446954

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
EduktTriethylamineHCID 8471—
Edukt2,2-DimethoxyethylmethylamineHCID 8503—
EduktCalcium ChlorideHCID 5284359—
LösungsmittelDiethyl EtherHCID 3283—
LösungsmittelDichloromethaneHCID 6344—
Produkt2-Chloro-N-(2,2-dimethoxyethyl)-N-methylacetamideHCID 12850700—

Reaktionsbedingungen

Temperatur-20 °C

Reaktionsschritte

N-Methyl-2,2-dimethoxyethanamine (50.0 grams; 0.42 mole), methylene chloride (200 ml) and triethylamine (46.6 grams; 0.462 mole) were charged into a glass reaction vessel fitted with a mechanical stirrer, and thermometer. A calcium chloride filled drying tube was attached and the solution was cooled to about -20° C. Chloroacetyl chloride (49.7 grams; 0.44 moles) dissolved in methylene chloride (25 ml) was then added dropwise, with stirring, while holding the temperature at about -20° C. to -10° C. At the end of the addition, stirring was continued at -20° C. to 10° C. for a period of about 1 hour. The solution was allowed to warm to room temperature, then was stirred at this temperature for a period of about 16 hours. Diethyl ether (125 ml) was then added and the resulting solution filtered. The filtrate was washed with water (30 ml). The washed filtrate was dried and filtered. The solvent was distilled off under mild heat and reduced pressure to yield a residue which was fractionally distilled under reduced pressure to yield the desired product N-methyl-N-(2,2-dimethoxyethyl)-2-chloroacetamide as a fraction boiling at 112° C.-119° C. at 0.30 mm. Hg.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04314840
Quelldatensatzuspto-grants-1982_02
ORD IDord-2303ad06abbf4883a1c21492113402da
Quellennotizuspto-grants-1982_02