HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Hydrogen Bromide → N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Hydrogen Bromide | HCID 260 | — |
| Edukt | N-(4-(4-(Ethylheptylamino)butyl)phenyl)methanesulfonamide | HCID 9864094 | — |
| Lösungsmittel | Diethyl Ether | HCID 3283 | — |
| Produkt | N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide | HCID 70387710 | 37% |
Reaktionsschritte
N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide (5.56 g, 0.015 mol), prepared according to the general procedure outlined in Example 1, was dissolved in diethyl ether. The solution was cooled with a dry ice/acetone bath and diethyl ether saturated with hydrogen bromide gas was added thereto. The volatiles were evaporated under reduced pressure and 100 ml of ethyl acetate was added to the residue. The solution was triturated and approximately 6 grams of crystals were collected. The solid was recrystalized from isopropyl alcohol to provide 2.5 g of N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide. mp=98°-100° C. Yield 37%
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US04596827 |
| Quelldatensatz | uspto-grants-1986_06 |
| ORD ID | ord-70253ae8ff4f441392973bf47651d6ac |
| Quellennotiz | uspto-grants-1986_06 |