HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1702498Erstellt: 26. Oktober 2026
Carbon Dioxide → N1-(3-chlorophenyl)ethane-1,2-diamine
https://huagongshe.com/reaction/1702498
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Carbon Dioxide | HCID 280 | — |
| Edukt | Hydrochloric Acid | HCID 313 | — |
| Edukt | 3-Chloroaniline | HCID 7932 | — |
| Edukt | Benzenamine, 3-chloro-, hydrochloride (1:1) | HCID 67336 | — |
| Edukt | 2-Oxazolidinone | HCID 73949 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | N1-(3-chlorophenyl)ethane-1,2-diamine | HCID 11008376 | 80% |
Reaktionsschritte
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.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04381401 |
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| Quelldatensatz | uspto-grants-1983_04 |
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| ORD ID | ord-4bf60c0eb8284bb6b3abd21ffe2f09cc |
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| Quellennotiz | uspto-grants-1983_04 |
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