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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 52660Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-Amino-5-(4-chlorophenoxy)benzonitrile

https://huagongshe.com/de/reaction/52660

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktWaterHCID 962—
Edukt2-Nitro-5-(4-chlorophenoxy)benzonitrileHCID 21824874—
KatalysatorIronHCID 23925—
LösungsmittelEthanolHCID 702—
Produkt2-Amino-5-(4-chlorophenoxy)benzonitrileHCID 218248519,1%

Reaktionsschritte

A mixture of 2.0 grams (0.035 mole) of iron powder, 1.0 mL of concentrated hydrochloric acid, 4.0 mL of water, in 30 mL of ethanol was stirred, and 2.5 grams (0.009 mole) of 2-nitro-5-(4-chlorophenoxy)benzonitrile was added slowly. Upon completion of addition, the reacton mixture was warmed to reflux where it stirred for about seven hours. After this time, the reaction mixture was allowed to cool to ambient temperature where it stirred for about 18 hours. The reaction mixture was then warmed and filtered through a pad of diatomaceous earth. The filtrate was concentrated under reduced pressure to a residue. The residue was purified with column chromatography on silica gel, using 1:1 petroleum ether/methylene chloride. The product-containing fractions were combined and concentrated under reduced pressure, yielding 0.2 gram of 2-amino-5-(4-chlorophenoxy)benzonitrile, mp 116°-118° C. The NMR spectrum was consistent with the proposed structure. The reaction was repeated.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05616718
Quelldatensatzuspto-grants-1997_04
ORD IDord-14cc633eef844e6188551abd518bf919
Quellennotizuspto-grants-1997_04