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
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Edukt | Triethylamine | HCID 8471 | — |
| Edukt | 4-((3-Hydroxypropyl)amino)benzonitrile | HCID 21867663 | — |
| Lösungsmittel | Acetonitrile | HCID 6342 | — |
| Produkt | 3-(4-Cyanoanilino)propyl 4-methylbenzenesulfonate | HCID 21867652 | 77,2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US06559143B1 |
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| Quelldatensatz | uspto-grants-2003_05 |
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| ORD ID | ord-9129a75e560848a78554a25f0f575611 |
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| Quellennotiz | uspto-grants-2003_05 |
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