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HRID 33372作成日:2026年10月25日

3-(3-methyl-3-nitro-butyl)-3H-benzoxazol-2-one → 3-(3-amino-3-methyl-butyl)-3H-benzoxazol-2-one

https://huagongshe.com/reaction/33372

反応式

関与物質

役割名称HCID仕込み量
反応物3-(3-methyl-3-nitro-butyl)-3H-benzoxazol-2-oneHCID 57435840—
触媒NickelHCID 935—
溶媒EthanolHCID 702—
生成物3-(3-amino-3-methyl-butyl)-3H-benzoxazol-2-oneHCID 57435838—

反応手順

11.0 g 3-(3-methyl-3-nitro-butyl)-3H-benzoxazol-2-one from the reaction described above are dissolved in 130 mL ethanol and hydrogenated with Raney nickel as catalyst at 5 bar for 20 hours. The catalyst is filtered off and the filtrate is freed from the solvent. 10% ethanolic hydrochloric acid is added, the solvent is distilled off and the residue is stirred in an acetone/diethyl ether mixture. White solid. Yield: 6.0 g (77% over 2 steps, hydrochloride); melting range=145-147° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429583B2
出典データセットuspto-grants-2008_09
ORD IDord-c0abc04fb7094e70a537e169bf77c463
出典メモuspto-grants-2008_09