HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrazine → N-(4-aminobenzyl)ethanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | N-(4-nitrobenzyl)ethanesulfonamide | HCID 47372696 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(4-aminobenzyl)ethanesulfonamide | HCID 39243426 | — |
Reaction Steps
To the residue of the product from step 1 (0.25 mmol) is added methanol (350 μL), hydrazine (33 μL), and Raney-Nickel (10 mg). The reaction mixture is shaken at room temperature for 16 hours, then filtered and the solution concentrated to yield ethanesulfonic acid 4-amino-benzylamide, which is used as such for the subsequent reaction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07713994B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-56f987b31f4c49e5bdcb88db96800530 |
| Source note | uspto-grants-2010_05 |