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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 411136Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktTriethylamineHCID 8471—
Edukt4-((3-Hydroxypropyl)amino)benzonitrileHCID 21867663—
LösungsmittelAcetonitrileHCID 6342—
Produkt3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonateHCID 2186765277,2%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06559143B1
Quelldatensatzuspto-grants-2003_05
ORD IDord-9129a75e560848a78554a25f0f575611
Quellennotizuspto-grants-2003_05