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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 326169생성일: 2026년 10월 25일

5-Amino-1-naphthol → 4-Fluoro-N-(5-hydroxynaphthalen-1-yl)-3-nitrobenzamide

https://huagongshe.com/reaction/326169

반응식

참여 물질

역할이름HCID투입량
반응물5-Amino-1-naphtholHCID 65746—
반응물4-Fluoro-3-nitrobenzoyl chlorideHCID 2783347—
용매N,N-DimethylanilineHCID 949—
용매AcetonitrileHCID 6342—
생성물4-Fluoro-N-(5-hydroxynaphthalen-1-yl)-3-nitrobenzamideHCID 20462598—

반응 조건

온도50 °C

반응 단계

22.4 g of 3-nitro-4-fluorobenzoyl chloride (0.12 mols) were added dropwise at 0° C. to a suspension of 19.1 g of 5-amino-1-naphthol (0.12 mols) in 120 ml of acetonitrile and 14.2 g of N,N-dimethylaniline. The mixture was further stirred until it reached room temperature, and then heated for 30 minutes at 50° C. The yellow deposit was suction filtered and washed with acetonitrile. The deposit was dissolved in tetrahydrofurane and stirred with charcoal, filtered and the product was precipitated from the filtrate with petrol 50/75. Yield: 25.8 g=66% of the theoretical yield; mp. 235°-238° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04444867
출처 데이터셋uspto-grants-1984_04
ORD IDord-6d33a443335a4931be334c29a34512c5
출처 메모uspto-grants-1984_04