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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 49932생성일: 2026년 10월 24일

Triethylamine → 4-Amino-1-naphthoic acid

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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Sodium HydroxideHCID 14798—
반응물4-Bromo-1-naphthylamineHCID 75303—
반응물Methyl 4-aminonaphthalene-1-carboxylateHCID 10821944—
촉매HCID 178418476HCID 178418476—
용매EthanolHCID 702—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
용매HCID 178418416HCID 178418416—
생성물4-Amino-1-naphthoic acidHCID 459314—

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06710056B2
출처 데이터셋uspto-grants-2004_03
ORD IDord-5698eedece90432c9b83a625bb4512b2
출처 메모uspto-grants-2004_03