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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 49932Generated: October 25, 2026

Triethylamine → 4-Amino-1-naphthoic acid

https://huagongshe.com/reaction/49932

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium HydroxideHCID 14798—
Reactant4-Bromo-1-naphthylamineHCID 75303—
ReactantMethyl 4-aminonaphthalene-1-carboxylateHCID 10821944—
CatalystHCID 178418476HCID 178418476—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventHCID 178418416HCID 178418416—
Product4-Amino-1-naphthoic acidHCID 459314—

Reaction Conditions

Temperature80 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06710056B2
Source datasetuspto-grants-2004_03
ORD IDord-5698eedece90432c9b83a625bb4512b2
Source noteuspto-grants-2004_03