戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 21451作成日:2026年10月23日

Water → 3-Fluoro-4-methylphenyl methyl sulfide

https://huagongshe.com/ja/reaction/21451

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-Fluoro-4-methylanilineHCID 9957—
反応物Tert-Butyl nitriteHCID 10906—
反応物Dimethyl DisulfideHCID 12232—
溶媒1,2-DichloroethaneHCID 11—
生成物3-Fluoro-4-methylphenyl methyl sulfideHCID 53414492525.5%

反応手順

A mixture of 3-fluoro-4-methylaniline (25 g), dimethyl disulphide (375 g) and t-butyl nitrite (30 ml) in 1,2-dichloroethane was warmed to start the reaction. A solution of 3-fluoro-4-methylaniline (225 g) in 1,2-dichloroethane was added dropwise, simultaneously with t-butyl nitrite (241 ml) at such a rate as to maintain the temperature below 60° C. The mixture was stirred for 2 hours, then water was added. The organic layer was washed with water, hydrochloric acid, dried (anhydrous magnesium sulphate) and filtered. The filtrate was evaporated to dryness and the residue was distilled to give 2-fluoro-4-(methylsulphenyl)toluene (164 g) as a yellow oil; NMR (acetone-d6); 2.2 (3H,d), 2.5 (3H,s), 7.05 (3H,m).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05424276
出典データセットuspto-grants-1995_06
ORD IDord-9b753ec268a24204821843de40f5cfd5
出典メモuspto-grants-1995_06