HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-Aminomethyl-N-tert-butyl-3-methyl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | N-tert-butyl-4-cyano-3-methylbenzenesulfonamide | HCID 58275375 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol hydrochloride | HCID 21887872 | — |
| Product | 4-Aminomethyl-N-tert-butyl-3-methyl-benzenesulfonamide | HCID 58275344 | 113.5% |
Reaction Steps
The reaction mixture of N-tert-butyl-4-cyano-3-methylbenzenesulfonamide (0.7176 g) and Pd/C (0.97 g) in 1N HCl/EtOH (1.5 ml 1N HCl in 15 ml EtOH) was stirred under H2 for 2 hours. Then 1N HCl (3 ml) was added to improve the reaction progress and it was stirred overnight. The reaction mixture was filtered through a pad of diatomaceous earth, washed with MeOH and concentrated to about 3 ml. The residue was diluted with H2O and lyophilized to give 0.8275 g 4-(aminomethyl)-N-tert-butyl-3-methylbenzenesulfonamide as white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08536187B2 |
| Source dataset | uspto-grants-2013_09 |
| ORD ID | ord-adae39ad027e4d13915efa2be87b76d5 |
| Source note | uspto-grants-2013_09 |