HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-(Methylthio)aniline → N-(4-difluoromethoxybenzylidene)-4-methylthioaniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-(Methylthio)aniline | HCID 66038 | — |
| Reactant | p-(Difluoromethoxy)benzaldehyde | HCID 2736986 | — |
| Product | N-(4-difluoromethoxybenzylidene)-4-methylthioaniline | HCID 21862828 | 91% |
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 | USRE039420E1 |
| Source dataset | uspto-grants-2006_12 |
| ORD ID | ord-ab7bb03df30745508dffe4180a92fe44 |
| Source note | uspto-grants-2006_12 |