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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 857184Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/857184

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 (a) 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
PatentnummerUS07144914B2
Quelldatensatzuspto-grants-2006_12
ORD IDord-7e4df5b77d394ed7ae15c96844f19730
Quellennotizuspto-grants-2006_12