HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 131325Generated: October 25, 2026
4-Fluoro-2-nitroaniline → 2-(4-Fluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile
https://huagongshe.com/reaction/131325
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoro-2-nitroaniline | HCID 67769 | — |
| Reactant | Lithium hydroxide, monohydrate | HCID 168937 | — |
| Reactant | 2-Fluoro-5-(trifluoromethyl)benzonitrile | HCID 521016 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(4-Fluoro-2-nitro-phenylamino)-5-trifluoromethyl-benzonitrile | HCID 21093461 | 96% |
Reaction Steps
Combine 4-fluoro-2-nitro-phenylamine (5.0 g, 32.03 mmol), 2-fluoro-5-trifluoromethyl-benzonitrile (6.07 g, 32.03 mmol) and lithium hydroxide monohydrate (4.03 g, 96.08 mmol) in methyl sulfoxide (DMSO, 60 ml). Heat the resulting mixture to 70° C. for 16 hours. Cool the reaction mixture to ambient temperature, then pour into approximately 400 ml of ice water and stir for one hour. Filter the resulting mixture and collect the precipitate to obtain 9.995 g of the title compound (30.73 mmol, 96% yield) as an orange amorphous solid. Product used as is with no further purification: Mass Spectrum (m/e): 326(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07384934B2 |
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| Source dataset | uspto-grants-2008_06 |
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| ORD ID | ord-709a5f8e5dfe4658858302fdd37086d6 |
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| Source note | uspto-grants-2008_06 |
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