HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trimethylsilyl cyanide → alpha-(4-Difluoromethoxyphenyl)-alpha-(4-methylthioanilino)acetonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | N-(4-difluoromethoxybenzylidene)-4-methylthioaniline | HCID 21862828 | — |
| Product | alpha-(4-Difluoromethoxyphenyl)-alpha-(4-methylthioanilino)acetonitrile | HCID 21862794 | — |
Reaction Steps
Following a procedure similar to that described in Example 1(i), but using 4-difluoromethoxybenzaldehyde and 4-methylthioaniline as starting materials, N-(4-difluoromethoxybenzylidene)-4-methylthioaniline was obtained in a yield of 91%. This aniline compound and trimethylsilyl cyanide were then reacted together in a similar manner to that described in Example 1(ii), to give the title compound as a slightly yellow powder (yield 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05908858 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-1acb421962b643b38a83edf095cf1104 |
| Source note | uspto-grants-1999_06 |