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HRID 404715作成日:2026年10月26日

4-Toluenesulfonyl chloride → N-(4-Bromo-benzyl)-N-(2,2-dimethoxy-ethyl)-4-methyl-benzenesulfonamide

https://huagongshe.com/reaction/404715

反応式

関与物質

役割名称HCID仕込み量
反応物4-Toluenesulfonyl chlorideHCID 7397—
反応物N-(4-Bromobenzyl)-2,2-dimethoxyethanamineHCID 59226241—
溶媒DichloromethaneHCID 6344—
溶媒Pyridine methylene chlorideHCID 21875418—
生成物N-(4-Bromo-benzyl)-N-(2,2-dimethoxy-ethyl)-4-methyl-benzenesulfonamideHCID 5922624563.4%

反応手順

60.5 g (4-Bromo-benzyl)-(2,2-dimethoxy-ethyl)-amine (1, crude product) were dissolved in 270 ml of dichloromethane/pyridine (8:1). At 0° C. a solution of 76.0 g (386.4 mmol) p-toluenesulfonylchloride in 100 ml of dichloromethane was added and the solution was stirred at room temperature. After 3 h, the reaction mixture was washed twice with 2 N HCl and saturated sodium hydrogen carbonate-solution. The organic layer was dried over magnesium sulfate and evaporated. Final silica gel chromatography (heptane/ethylacetate 4:1) gave 59.9 g of the title compound. Rt=1.82 min (Method C). Detected mass: 396.1/398.1 (M−OMe−).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08748614B2
出典データセットuspto-grants-2014_06
ORD IDord-29886b4c7422484ea3dc83b0874094f9
出典メモuspto-grants-2014_06