HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | N-(4-(4-(Ethylheptylamino)butyl)phenyl)methanesulfonamide | HCID 9864094 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide | HCID 70387710 | 37% |
Reaction Steps
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 appoximately 6 grams of crystals were collected. The solid was recrystallized from isopropyl alcohol to provide 2.5 g of N-[4-[4-(ethylheptylamino)butyl]phenyl]methanesulfonamide monohydrobromide. mp=98°-100° C. Yield 37%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04569801 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-6d749e6c337e414abdd3df98d3452654 |
| Source note | uspto-grants-1986_02 |