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HRID 605421作成日:2026年10月24日

2-Fluoroaniline → 2-Fluoro-4-thiocyanatoaniline

https://huagongshe.com/ja/reaction/605421

反応式

関与物質

役割名称HCID仕込み量
反応物2-FluoroanilineHCID 9584—
反応物BromineHCID 24408—
反応物Sodium thiocyanateHCID 516871—
反応物Sodium BicarbonateHCID 516892—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒Sodium bromide methanolHCID 20267117—
生成物2-Fluoro-4-thiocyanatoanilineHCID 435636586.2%

反応手順

2-Fluoroaniline (9.8 mL, 0.1 mol) and sodium thiocyanate (24.9 g, 0.3 mol) in MeOH (55 mL) were treated with a cold solution of bromine (5.7 mL, 0.11 mol) in saturated NaBr-MeOH solution (50 mL) added dropwise at −5-0° C. over 2 hours. After the addition, the reaction mixture was poured into cold water (200 mL) with stirring, adjusted to pH 8-9 with NaHCO3 (10 g), and stirred at 5° C. for 30 minutes. The resulting crystals were collected by filtration, washed with cold water, and dried at room temperature overnight in vacuum to give crude product 2-fluoro-4-thiocyanatoaniline (14.5 g) as slightly brown crystal. A mixture of the crude 2-fluoro-4-thiocyanatoaniline (14.5 g) and concentrated hydrochloric acid (58 mL) in EtOH (15 mL) was refluxed for 8 hours. The reaction mixture was cooled and stirred at room temperature overnight. The resulting crystals were collected by filtration, washed with cold EtOH and i-Pr2O, dried at room temperature overnight in vacuum to give the title compound as its hydrochloride salt (pale yellow crystal, 10.1 g, 56%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07910595B2
出典データセットuspto-grants-2011_03
ORD IDord-c24c06d0fcf942ecb7625a9a994ae638
出典メモuspto-grants-2011_03