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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397518Generated: October 30, 2026

4-(3-Ethynylphenoxy)-1,2-dinitrobenzene → 4-(3-Ethynylphenoxy)benzene-1,2-diamine

https://huagongshe.com/reaction/2397518

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(3-Ethynylphenoxy)-1,2-dinitrobenzeneHCID 20356952—
CatalystZincHCID 23994—
SolventTetrahydrofuranHCID 8028—
SolventAmmonium HydroxideHCID 14923—
Product4-(3-Ethynylphenoxy)benzene-1,2-diamineHCID 21326249—

Reaction Steps

To a rapidly stirred suspension of 25 g (0.38 g atom) of powdered zinc in 25 ml of concentrated ammonium hydroxide was added a solution containing 5.0 g (17.6 mmoles) of 4-(3-ethynylphenoxy)-o-dinitrobenzene dissolved in 25 ml of tetrahydrofuran. The mixture was stirred at room temperature for 1/2 hour, at which time an additional 5 ml of ammonium hydroxide was added, and the solution stirred an additional half hour. At that time, the reaction mixture was filtered by suction, and the residue was washed with several portions of tetrahydrofuran. The filtrate was extracted with several portions of ether, and the combined ether extracts washed with water. Evaporation of the organic layer in vacuo yielded a dark red oil. Chromatography of the residue on 1" × 12" dry column of silica gel afforded an initial red band (elution with methylene chloride) of side-product. Further elution using ethyl acetate produced a second band of desired product. Evaporation of solvent in vacuo yielded 3.3 g (84%) of 4-(3-ethynylphenoxy)-o-phenylenediamine as a dark orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04022746
Source datasetuspto-grants-1977_05
ORD IDord-15cb924c28da4b64aca260fbd3a0ff66
Source noteuspto-grants-1977_05