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HRID 510150作成日:2026年10月25日

Ethyl Acetate → 4-[(4-Fluorophenyl)sulfanyl]aniline

https://huagongshe.com/reaction/510150

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Ammonium ChlorideHCID 25517—
反応物1-Fluoro-4-[(4-nitrophenyl)sulfanyl]benzeneHCID 2783059—
触媒IronHCID 23925—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒TetrahydrofuranHCID 8028—
生成物4-[(4-Fluorophenyl)sulfanyl]anilineHCID 277474085%

反応条件

温度75 °C

反応手順

To a solution of ammonium chloride (16.63 g, 311 mmol) in water (300 mL) are added iron (17.39 g, 311 mmol) and a solution of 1-fluoro-4-(4-nitrophenyl)sulfanyl-benzene (19.40 g, 78 mmol) in a mixture of methanol (100 mL) and tetrahydrofuran (100 mL). The resulting mixture is heated to 75° C. for 2.5 h and then cooled to room temperature. After addition of ethyl acetate (1 L), the mixture is stirred for 10 min the organic layer is decanted and collected. This procedure is repeated twice. The combined organic layers are dried over sodium sulphate, filtered and concentrated under reduced pressure. The crude residue is first triturated twice with diethyl ether and then purified via column chromatography on silica gel (heptane/ethyl acetate 0 to 30% as eluent) to afford the desired product as a yellow solid (14.45 g, 66 mmol, 85% yield) (HPLC-MS Method 2: retention time: 1.939 min, m/z 261.0).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096599B2
出典データセットuspto-grants-2015_08
ORD IDord-0d313d4c469b4913ad6bd87353d98241
出典メモuspto-grants-2015_08