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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1702498Generated: October 26, 2026

Carbon Dioxide → N1-(3-chlorophenyl)ethane-1,2-diamine

https://huagongshe.com/reaction/1702498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantHydrochloric AcidHCID 313—
Reactant3-ChloroanilineHCID 7932—
ReactantBenzenamine, 3-chloro-, hydrochloride (1:1)HCID 67336—
Reactant2-OxazolidinoneHCID 73949—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
ProductN1-(3-chlorophenyl)ethane-1,2-diamineHCID 1100837680%

Reaction Conditions

Temperature160 °C

Reaction Steps

Gaseous hydrogen chloride was reacted with m-chloroaniline in ether at 0° C. to prepare the m-chloroaniline hydrochloride. This reactant (65.6 g, 0.4 mole) was then intimately mixed with 2-oxazolidinone by grinding with a mortar and pestle. The ground mixture was then added to a 250 ml flask equipped with a mechanical stirrer and gas vent. The flask was heated in an oil bath to 160° C. with stirring. The solid mixture melted and CO2 evolution commenced in about 15 minutes. Heating was continued for about six hours whereupon the flask was cooled and the contents dissolved in water and filtered. The filtrate was then basified with aqueous caustic causing a yellow oil to separate. Extraction with methylene chloride, drying and distillation under vacuum gave 55 g (80 percent yield) of N-(3-chlorophenyl)-1,2-ethanediamine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04381401
Source datasetuspto-grants-1983_04
ORD IDord-4bf60c0eb8284bb6b3abd21ffe2f09cc
Source noteuspto-grants-1983_04