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HRID 427609作成日:2026年10月26日

Sodium borohydride → 3-Benzyloxy-4-methyl-phenylamine

https://huagongshe.com/reaction/427609

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium borohydrideHCID 4311764—
反応物2-Benzyloxy-1-methyl-4-nitro-benzeneHCID 18174502—
触媒Nickel acetate tetrahydrateHCID 62601—
溶媒MethanolHCID 887—
溶媒TetrahydrofuranHCID 8028—
生成物3-Benzyloxy-4-methyl-phenylamineHCID 279462597%

反応条件

温度0 °C

反応手順

To a stirred solution of 3-benzyloxy-4-methylnitrobenzene (1.1 g, 4.4 mmol) in tetrahydrofuran (25 mL) and methanol (50 mL) was added nickel acetate tetrahydrate (2.2 g, 8.7 mmol). The solution was cooled to 0° C. and sodium borohydride (0.66 g, 17.4 mmol) was added in small portions. After gas evolution had ceased, the solvents were removed in vacuo and the residue was partitioned between ethyl acetate and concentrated ammonium hydroxide. The layers were separated and the organic phase was washed with ammonium hydroxide followed by saturated aqueous sodium chloride solution, dried (magnesium sulfate), filtered, and concentrated In vacuo to give 0.9 g (97%) of the title product as an off-white solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06313122B1
出典データセットuspto-grants-2001_11
ORD IDord-8c3d28d6a97640429c7e8a64d414bdb4
出典メモuspto-grants-2001_11