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HRID 500468作成日:2026年10月26日

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

https://huagongshe.com/reaction/500468

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US07772229B2
出典データセットuspto-grants-2010_08
ORD IDord-e06da6fe63584a4b92e67124f919436f
出典メモuspto-grants-2010_08