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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 267455Erstellt: 25. Oktober 2026

Chloroacetyl chloride → N-alpha-chloroacetyl-N-(1,3-dioxolan-2-ylmethyl)-2,6-dimethylaniline

https://huagongshe.com/reaction/267455

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktChloroacetyl chlorideHCID 6577—
Edukt1,4-DioxaneHCID 31275—
Edukt1,3-Dioxolane-2-methanamine, N-(2,6-dimethylphenyl)-HCID 104710—
EduktSodium BicarbonateHCID 516892—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
ProduktN-alpha-chloroacetyl-N-(1,3-dioxolan-2-ylmethyl)-2,6-dimethylanilineHCID 13017584—

Reaktionsschritte

N-(1,3-Dioxolan-2-ylmethyl)-2,6-dimethylaniline (7.8 grams), sodium bicarbonate (7.0 grams), dioxane (20 ml) and water (4 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. The mixture was cooled to a temperature of about 0°C and chloroacetyl chloride (5.0 grams) was added, with stirring, over a period of about 15 minutes. After the addition was completed stirring was continued for a period of about one hour. After this time ether (100 ml) was added to the mixture and the resulting solution was washed with water. The washed solution was then dried over anhydrous magnesium sulfate and stripped of solvents leaving a solid residue. The residue was recrystallized from an ether-pentane mixture to yield the desired product N-α-chloroacetyl-N-(1,3-dioxolan-2-ylmethyl)-2,6-dimethylaniline having a melting point of 58° to 60°C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS03942972
Quelldatensatzuspto-grants-1976_03
ORD IDord-745f08bdc6c048fa8071ba7471eca670
Quellennotizuspto-grants-1976_03