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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49932Erstellt: 24. Oktober 2026

Triethylamine → 4-Amino-1-naphthoic acid

https://huagongshe.com/de/reaction/49932

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktSodium HydroxideHCID 14798—
Edukt4-Bromo-1-naphthylamineHCID 75303—
EduktMethyl 4-aminonaphthalene-1-carboxylateHCID 10821944—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelEthanolHCID 702—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelHCID 178418416HCID 178418416—
Produkt4-Amino-1-naphthoic acidHCID 459314—

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

1.60 g (2.3 mmol) of bis(triphenylphosphine)dichloropalladium, 7.0 ml (50.6 mmol) of triethylamine and 60 ml of methanol were successively added to a mixture of 5.00 g (22.5 mmol) of 1-amino-4-bromonaphthalene and 60 ml of dimethylformamide, and they were stirred in carbon monoxide atmosphere at 80° C. for 2 days. After the concentration under reduced pressure, water was added to the reaction mixture and the product was extracted with ethyl acetate and concentrated. 20 ml of ethanol and 10 ml (40.0 mmol) of 4 N aqueous sodium hydroxide solution were added to crude methyl 4-amino-1-naphthalenecarboxylate thus obtained. They were stirred at 80° C. overnight. Ethanol was evaporated, and the residue was washed with ethyl acetate. The aqueous layer was neutralized with hydrochloric acid. After the extraction with ethyl acetate, the product was washed with water and saturated aqueous sodium chloride solution, dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06710056B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-5698eedece90432c9b83a625bb4512b2
Quellennotizuspto-grants-2004_03