HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfanilamide → 4-[(4-Ethoxybenzylidene)amino]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfanilamide | HCID 5333 | — |
| Reactant | 4-Ethoxybenzaldehyde | HCID 24834 | — |
| Product | 4-[(4-Ethoxybenzylidene)amino]benzenesulfonamide | HCID 690834 | — |
Reaction Steps
Following a procedure similar to that described in Example 1(i), but using 4-ethoxybenzaldehyde and 4-sulfamoylaniline as starting materials, the title compound was obtained as a pale yellow powder (yield 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05908858 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-3a8afc9ee4f840489c6de4a4c3279791 |
| Source note | uspto-grants-1999_06 |