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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1734622Generated: October 26, 2026

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

https://huagongshe.com/reaction/1734622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
Reactant2-Nitro-5-(4-chlorophenoxy)benzonitrileHCID 21824874—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product2-Amino-5-(4-chlorophenoxy)benzonitrileHCID 218248519.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05534518
Source datasetuspto-grants-1996_07
ORD IDord-04f05cdf149040049b50fc2fb88abf13
Source noteuspto-grants-1996_07