Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605043Generated: October 25, 2026

Chloroacetyl chloride → N-alpha-chloroacetyl-N-(1,3-dioxolan-2-ylmethyl)-2-methyl-5-chloroaniline

https://huagongshe.com/reaction/1605043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant1,4-DioxaneHCID 31275—
ReactantSodium BicarbonateHCID 516892—
ReactantN-(1,3-Dioxolan-2-ylmethyl)-2-methyl-5-chloroanilineHCID 21548992—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductN-alpha-chloroacetyl-N-(1,3-dioxolan-2-ylmethyl)-2-methyl-5-chloroanilineHCID 21549007—

Reaction Steps

N-(1,3-Dioxolan-2-ylmethyl)-2-methyl-5-chloroaniline (8 grams), sodium bicarbonate (7 grams), dioxane (50 ml) and water (4 ml) were charged into a glass reaction vessel equipped with a mechanical stirrer and thermometer. This mixture was cooled to a temperature of about 0°C and chloroacetyl chloride (4.3 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 1 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 hexane to yield the desired product N-α-chloroacetyl-N-(1,3-dioxolan-2-ylmethyl)-2-methyl-5-chloroaniline having a melting point of 88° to 89°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03948950
Source datasetuspto-grants-1976_04
ORD IDord-2a0a617f247d4661a5afb2063ef3fd69
Source noteuspto-grants-1976_04