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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 379690Erstellt: 24. Oktober 2026

Nitric Acid → 2-Cyclopropylaniline

https://huagongshe.com/de/reaction/379690

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktNitric AcidHCID 944—
EduktSodium HydroxideHCID 14798—
EduktCyclopropylbenzeneHCID 70112—
Edukt1-Cyclopropyl-4-nitrobenzeneHCID 312713—
Edukt1-Nitro-2-phenylcyclopropaneHCID 12551046—
KatalysatorAdams' catalystHCID 345198—
LösungsmittelEthanolHCID 702—
LösungsmittelAcetic AnhydrideHCID 7918—
Produkt2-CyclopropylanilineHCID 76618—

Reaktionsschritte

A solution of 5 g (42 mmol) of cyclopropylbenzene in 20 ml of acetic anhydride is cooled to 15° C. While keeping the temperature below 20° C., 3.7 ml of 68% nitric acid are added slowly. The reaction mixture is stirred for one hour at that temperature, hydrolysed, rendered alkaline with 2N sodium hydroxide solution and extracted twice with 100 ml of ether. The organic phase is then dried and concentrated to yield a mixture of 2-nitrocyclo-propylbenzene and 4-nitrocyclopropylbenzene. The mixture is dissolved in 15 ml of ethanol and hydrogenated at normal temperature and pressure in the presence of 50 mg of PtO2. The residue obtained after filtering off the catalyst and evaporating off the solvent is purified by chromatography on silica gel to yield the title product.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06300366B1
Quelldatensatzuspto-grants-2001_10
ORD IDord-29265d846b3847d3971aad7b8a174bcc
Quellennotizuspto-grants-2001_10