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HRID 578778作成日:2026年10月27日

Water → 3-(1-Methyl-1-phenylethylthio)nitrobenzene

https://huagongshe.com/reaction/578778

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Alpha-MethylstyreneHCID 7407—
反応物3-Nitrobenzene-1-thiolHCID 243576—
溶媒TetrahydrofuranHCID 8028—
生成物3-(1-Methyl-1-phenylethylthio)nitrobenzeneHCID 68995809100.1%

反応手順

To a mixed solution of water (1.6 mL)-concentrated sulfuric acid (1.6 mL) was added 3-nitrothiophenol (0.5 g), and the mixture was stirred at room temperature for 1 hour. To the mixture was added a solution of α-methylstyrene (0.38 g) in tetrahydrofuran (1.6 mL), and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was poured into ice water, and the resulting mixture was extracted with ethyl acetate. The extract was washed with water, a saturated aqueous sodium hydrogen carbonate solution and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane−n-hexane/ethyl acetate=3/2) to give 3-(1-methyl-1-phenylethylthio)nitrobenzene (0.88 g). This material was dissolved in tetrahydrofuran (10 mL). To the solution were added methanol (10 mL), nickel (II) bromide (35 mg) and sodium borohydride (0.37 g) under ice-cooling, and the mixture was stirred at the same temperature for 30 minutes. Then the mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with ethyl acetate, and the resulting mixture was washed with a saturated aqueous sodium hydrogen carbonate solution, water and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane−n-hexane/ethyl acetate=3/2) to give the title compound (0.69 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09040693B2
出典データセットuspto-grants-2015_05
ORD IDord-f12a09ac2f784448b244e4667d8b0345
出典メモuspto-grants-2015_05