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HRID 49932作成日:2026年10月26日

Triethylamine → 4-Amino-1-naphthoic acid

https://huagongshe.com/reaction/49932

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Sodium HydroxideHCID 14798—
反応物4-Bromo-1-naphthylamineHCID 75303—
反応物Methyl 4-aminonaphthalene-1-carboxylateHCID 10821944—
触媒HCID 178418476HCID 178418476—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒DimethylformamideHCID 6228—
溶媒HCID 178418416HCID 178418416—
生成物4-Amino-1-naphthoic acidHCID 459314—

反応条件

温度80 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06710056B2
出典データセットuspto-grants-2004_03
ORD IDord-5698eedece90432c9b83a625bb4512b2
出典メモuspto-grants-2004_03