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HRID 411136作成日:2026年10月24日

4-Toluenesulfonyl chloride → 3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonate

https://huagongshe.com/ja/reaction/411136

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TriethylamineHCID 8471—
反応物4-((3-Hydroxypropyl)amino)benzonitrileHCID 21867663—
溶媒AcetonitrileHCID 6342—
生成物3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonateHCID 2186765277.2%

反応条件

温度0 °C

反応手順

A cooled (0° C.) solution of 4-[(3-hydroxypropyl)amino]benzonitrile (from step (i) above; 17 g, 96.5 mmol) in dry MeCN (195 mL) was treated with triethylamine (9.8 g, 96.5 mmol) and then p-toluenesulfonyl chloride (20.2 g, 106 mmol). The mixture was stirred at 0° C. for 90 minutes before being concentrated in vacuo. Water (200 mL) was added to the residue, and the aqueous solution was extracted with DCM. The organic phase was dried (Na2SO4), filtered and concentrated in vacuo. The resulting residue was purified by crystallisation from iso-propanol to yield 24.6 g (77%) of the sub-title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06559143B1
出典データセットuspto-grants-2003_05
ORD IDord-9129a75e560848a78554a25f0f575611
出典メモuspto-grants-2003_05