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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411523생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/411523

반응식

참여 물질

역할이름HCID투입량
반응물4-Toluenesulfonyl chlorideHCID 7397—
반응물TriethylamineHCID 8471—
반응물4-((3-Hydroxypropyl)amino)benzonitrileHCID 21867663—
용매AcetonitrileHCID 6342—
생성물3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonateHCID 2186765277.2%

반응 조건

온도0 °C

반응 단계

A cooled (0° C.) solution of 4-[(3-hydroxypropyl)amino]benzonitrile (see 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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06559162B2
출처 데이터셋uspto-grants-2003_05
ORD IDord-725ce140320b4f1db7a541b4a9cda6d0
출처 메모uspto-grants-2003_05