HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(4-Nitrobenzyl)cyclopropanesulfonamide → N-(4-Aminobenzyl)cyclopropanesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(4-Nitrobenzyl)cyclopropanesulfonamide | HCID 66910210 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(4-Aminobenzyl)cyclopropanesulfonamide | HCID 64552598 | — |
Reaction Steps
N-Cyclopropylsulfonyl-4-nitrobenzylamine was dissolved in methanol (50 mL) and to the solution was added 10% Pd—C. The reaction mixture was placed under hydrogen atmosphere (˜40 psi) and shaken for 1 h. The catalyst was filtered off over celite and washed with methanol (1 L) and water (10 mL). The filtrate was evaporated to give N-cyclopropylsulfonyl-4-aminobenzylamine. 1H NMR (DMSO-d6): δ 0.87 (m, 4H), 2.37 (m, 1H), 3.96 (d, J=6.0 Hz, 2H), 4.99 (br, 2H), 6.49 (d, J=8.1 Hz, 2H), 6.96 (d, J=8.4 Hz, 2H), 7.33 (t, J=6.0 Hz, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09040543B2 |
| Source dataset | uspto-grants-2015_05 |
| ORD ID | ord-f16ae27b9c644dbdb7207f9cdb78784f |
| Source note | uspto-grants-2015_05 |