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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876197Generated: October 30, 2026

Hydrochloric Acid → 1-Amino-4(1,8-nonadiene-5-yloxy)benzene

https://huagongshe.com/reaction/876197

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
Reactant1-Nitro-4-(1,8-nonadiene-5-yloxy)benzeneHCID 86708878—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
Product1-Amino-4(1,8-nonadiene-5-yloxy)benzeneHCID 86708879688.6%

Reaction Steps

A 300 ml-capacity three neck flask containing a stirring bar and connected to a condenser was sufficiently dried. Then, a nitrogen atmosphere was established in the flask. 1-nitro-4-(1,8-nonadiene-5-yloxy)benzene (11) (4.01 g, 1.4 mmol), an iron powder (3.13 g, 5.6 mmol), and ethanol (50%, 10 ml) were introduced into the flask, and the mixture thus obtained was started to be stirred while heating the flask in an oil bath. Further, HCl (0.52 ml) and ethanol (50%, 2.5 ml) were slowly added to the mixture, which was then stirred for 2 hours. Thereafter, an aqueous sodium hydroxide solution was added to the mixture to stop the reaction, and an organic layer was extracted with ethyl acetate. This organic layer was dried over Na2SO4 and filtered, a solvent was distilled of under reduced pressure, and the organic layer was purified by flash chromatography on silica gel (hexane:ethyl acetate=10:1). Thus, 1-amino-4(1,8-nonadiene-5-yloxy)benzene (12) (2.39 g, 9.64×10−3 mol, yield: 69%) was obtained as an intended compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987044B2
Source datasetuspto-grants-2015_03
ORD IDord-6eb22a9fa07b4162a0af5932d1b74519
Source noteuspto-grants-2015_03