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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 494920Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-Allyloxy-4-methoxyaniline

https://huagongshe.com/reaction/494920

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTetrahydrofuranHCID 8028—
EduktAmmonium ChlorideHCID 25517—
Edukt2-Allyloxy-4-methoxynitrobenzeneHCID 10330708—
KatalysatorIronHCID 23925—
LösungsmittelEthanolHCID 702—
LösungsmittelWaterHCID 962—
Produkt2-Allyloxy-4-methoxyanilineHCID 5768291660,9%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

2.09 g of 2-allyloxy-4-methoxynitrobenzene was dissolved in 20 ml of ethanol, 5 ml of THF, and 4 ml of water. Thereafter, 4.27 g of ammonium chloride and 2.23 g of iron were added to the reaction solution, and the obtained mixture was stirred while heating at 80° C. for 4 hours. Thereafter, 2 g of ammonium chloride, 1 g of iron, and 0.25 ml of 5 N HCl were added to the reaction solution, and the obtained mixture was further stirred while heating for approximately 2 hours. The reaction solution was stood to cool and then filtered through celite. A saturated sodium bicarbonate aqueous solution and ethyl acetate were added thereto, so as to separate an organic layer. The obtained organic layer was washed with a saturated sodium chloride solution and then dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the organic layer was concentrated under a reduced pressure, and the residue was then purified by NH silica gel column chromatography (hexane/ethyl acetate), so as to obtain 1.09 g of the subject compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07538123B2
Quelldatensatzuspto-grants-2009_05
ORD IDord-2e12f6eb102f4041bb915e4f8be842b7
Quellennotizuspto-grants-2009_05