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HRID 903980作成日:2026年10月26日

Hydrochloric Acid → N-(5-Hydroxynaphthalen-1-yl)-2-methylprop-2-enamide

https://huagongshe.com/reaction/903980

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium CarbonateHCID 10340—
反応物Methacryloyl chlorideHCID 13528—
反応物5-Amino-1-naphtholHCID 65746—
触媒4-MethoxyphenolHCID 9015—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒PyridineHCID 1049—
生成物N-(5-Hydroxynaphthalen-1-yl)-2-methylprop-2-enamideHCID 1979996487.8%

反応条件

温度-10 °C

反応手順

Into a mixture comprising 227 g of 5-amino-α-naphthol, 1 g of hydroquinone monomethyl ether and 2 liters of pyridine was dropwise added with stirring 110 g of methacrylic acid chloride cooled to -10° C. by the use of a coolant. After completion of the addition, the mixture was stirred at 0°-3° C. for 2 hours, followed by stirring at 25° C. for 2 hours. Thereafter, the reaction liquid was poured into 20 liters of water to form a precipitate which was then filtered, water-washed and then dried to obtain solids. The solids were added to 2 liters of a 1:1 mixture of methanol and a 5% sodium carbonate solution, and after stirring at 40° C. the mixture was poured into 4 liters of a 5% hydrochloric acid to form a large amount of precipitate. The precipitate was filtered by suction and then recrystallized from ethanol to obtain 210 g of N-(5-hydroxy-α-naphthyl)methacrylamide, m.p. 223°-224° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04229514
出典データセットuspto-grants-1980_10
ORD IDord-3d8de8fd46fc46848278ac069620c27c
出典メモuspto-grants-1980_10