HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-2-nitroaniline → 2-(4-Chloro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-2-nitroaniline | HCID 6979 | — |
| Reactant | 2-Fluoro-5-(trifluoromethyl)benzonitrile | HCID 521016 | — |
| Product | 2-(4-Chloro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile | HCID 58625992 | 95% |
Reaction Steps
Using a method similar to Example 39, using 4-chloro-2-nitro-phenylamine (6.4 g, 37.3 mmol), 2-fluoro-5-trifluoromethyl-benzonitrile (7.05 g, 37.3 mmol) to obtain 12.03 g of the title compound (95% yield) as an amorphous yellow solid. Product can be used as is with no further purification: Mass Spectrum (m/e): 342(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07384934B2 |
| Source dataset | uspto-grants-2008_06 |
| ORD ID | ord-3b5cb89fabd84709bb6d39d0840549fc |
| Source note | uspto-grants-2008_06 |