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HRID 257598作成日:2026年10月24日

1-Nitronaphthalene → 4-Nitro-1-naphthylamine

https://huagongshe.com/ja/reaction/257598

反応式

関与物質

役割名称HCID仕込み量
反応物1-NitronaphthaleneHCID 6849—
反応物Potassium HydroxideHCID 14797—
反応物Ammonium ChlorideHCID 25517—
溶媒Dimethyl SulfoxideHCID 679—
生成物4-Nitro-1-naphthylamineHCID 13057—

反応手順

3.5 g of 1-nitronaphthalene and 3.3 g of N,N-tetramethylenethiocarbamoylsulphenamide, dissolved in 15 ml of dimethyl sulphoxide, are added dropwise to a vigorously stirred suspension of 6 g of potassium hydroxide in 50 ml of dimethyl sulphoxide, the temperature being kept at 20° to 25° C. When the addition has ended the mixture is stirred for a further 60 minutes, poured into 400 ml of a saturated aqueous ammonium chloride solution and extracted with methylene chloride. After drying and removing the solvent, 4-nitro-1-naphthylamine is obtained with a melting point of 190° to 192° C. The yield is 2.9 g (77%). 1Nitro-2-napthylamine is additionally obtained in a yield of about 2%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05262539
出典データセットuspto-grants-1993_11
ORD IDord-7974db6dad9b4a9cad76e2dd880c957c
出典メモuspto-grants-1993_11