HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl cyanide → alpha-(3,4-Dimethylanilino)-alpha-(4-sulfamoylphenyl)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | 3,4-Dimethyl-N-(4-sulfamoylbenzylidene)aniline | HCID 21862755 | — |
| Product | alpha-(3,4-Dimethylanilino)-alpha-(4-sulfamoylphenyl)acetonitrile | HCID 21862804 | — |
Reaction Steps
Following a procedure similar to that described in Example 1(ii), but using 3,4-dimethyl-N-(4-sulfamoylbenzylidene)aniline [prepared as described in step (i) above] and trimethylsilyl cyanide as starting materials, the title compound was obtained as a yellow powder (yield 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05908858 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-08c67afe61a747f5b1e7d546551b997e |
| Source note | uspto-grants-1999_06 |