HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Diisopropylethylamine → N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Trifluoromethylbenzenesulphonyl chloride | HCID 136616 | — |
| Edukt | (5-Bromothiophen-2-yl)methanamine | HCID 23130577 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Produkt | N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide | HCID 35408897 | 57,2% |
Reaktionsschritte
To a stirred suspension of 1-(5-bromo-2-thienyl)-methanamine (0.5 g) in dichloromethane (8 mL) were added 2-(trifluoromethyl)-benzenesulfonyl chloride (0.67 g) and N-ethyl-diisopropylamine (0.37 g) at 0° C. After stirring for 10 min, the ice bath was removed and the mixture was stirred for 40 min. The reaction mixture was diluted with dichloromethane and washed with 0.5 M HCl and with water. The organic phase was dried (MgSO4), filtered and concentrated. The residue was suspended in cyclohexane. The solid was collected by filtration and dried to give N-(5-bromo-thiophen-2-ylmethyl)-2-trifluoromethyl-benzenesulfonamide (0.596 g) as a colorless solid. MS: 417.1 ([M+NH4]+)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US08039493B2 |
| Quelldatensatz | uspto-grants-2011_10 |
| ORD ID | ord-dc894f865cda4f85bea1c75c570400e6 |
| Quellennotiz | uspto-grants-2011_10 |