HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-3-(trifluoromethyl)aniline → N-(Benzimidazol-2-yl)-4-chloro-3-(trifluoromethyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-3-(trifluoromethyl)aniline | HCID 67574 | — |
| Reactant | 2-Chlorobenzimidazole | HCID 78572 | — |
| Product | N-(Benzimidazol-2-yl)-4-chloro-3-(trifluoromethyl)aniline | HCID 923993 | — |
Reaction Steps
The title compound was prepared from 2-chlorobenzimidazole and 4-chloro-3-(trifluoromethyl)aniline by Procedure A. The product was isolated by filtration and recrystallisation to give the title compound as a hydrochloride salt (white solid, mp 255-260° C.). MS(ES+) m/z 312 ([M+1]+, 100).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07960561B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-65ac124bf4434342ab776c060ec5fb14 |
| Source note | uspto-grants-2011_06 |