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HRID 326169作成日:2026年10月26日

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

https://huagongshe.com/reaction/326169

反応式

関与物質

役割名称HCID仕込み量
反応物5-Amino-1-naphtholHCID 65746—
反応物4-Fluoro-3-nitrobenzoyl chlorideHCID 2783347—
溶媒N,N-DimethylanilineHCID 949—
溶媒AcetonitrileHCID 6342—
生成物4-Fluoro-N-(5-hydroxynaphthalen-1-yl)-3-nitrobenzamideHCID 20462598—

反応条件

温度50 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04444867
出典データセットuspto-grants-1984_04
ORD IDord-6d33a443335a4931be334c29a34512c5
出典メモuspto-grants-1984_04