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Trimethylsilyl cyanide → alpha-(4-Difluoromethoxyphenyl)-alpha-(4-methylthioanilino)acetonitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Trimethylsilyl cyanide | HCID 82115 | — |
| 反応物 | N-(4-difluoromethoxybenzylidene)-4-methylthioaniline | HCID 21862828 | — |
| 生成物 | alpha-(4-Difluoromethoxyphenyl)-alpha-(4-methylthioanilino)acetonitrile | HCID 21862794 | — |
反応手順
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%).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | USRE039420E1 |
| 出典データセット | uspto-grants-2006_12 |
| ORD ID | ord-57ad9aa7631f4021aea9c24dc81424f8 |
| 出典メモ | uspto-grants-2006_12 |