HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Methanesulfonyl chloride → N-(3-ethynylphenyl)methanesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Methanesulfonyl chloride | HCID 31297 | — |
| Edukt | Benzenamine, 3-ethynyl- | HCID 104682 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | N-(3-ethynylphenyl)methanesulfonamide | HCID 57131399 | — |
Reaktionsschritte
To a solution of 3-ethynyl aniline (1.05 mL, 10.0 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (857 μL, 1.10 eq.) at a temperature of 0° C. The resulting mixture was stirred overnight at room temperature and was then evaporated. The residue was treated with 2 N aq. HCl (25 mL) and subsequently extracted with ethyl acetate (2×30 mL). The combined organic layers were dried over MgSO4 and evaporated to give the desired methanesulfonamide in quantitative yield. It was used without further purification.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08524724B2 |
| Quelldatensatz | uspto-grants-2013_09 |
| ORD ID | ord-e04eb91ca7634a4a97f9b40e63bc61d3 |
| Quellennotiz | uspto-grants-2013_09 |