HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45064Generated: October 29, 2026
Acetic Acid → 3-Amino-5-(trifluoromethyl)benzonitrile
https://huagongshe.com/reaction/45064
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | 3-Cyano-5-nitrobenzotrifluoride | HCID 10727433 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Amino-5-(trifluoromethyl)benzonitrile | HCID 22502264 | 49.5% |
Reaction Steps
To a solution of 3-nitro-5-(trifluoromethyl)benzonitrile (500 mg, 2.31 mmol) and acetic acid (6.62 mL, 116 mmol) in EtOH (10 mL) and water (10 mL) is added tin (II) chloride (2.61 g, 11.6 mmol) and the reaction mixture is heated at 80° C. for 6 h. The solvent is removed in vacuo and then the residue is portioned between DCM and 4 N HCl solution. The organic layer separated and then dried over anhydrous Na2SO4, filtered and concentrated. The residue is then separated via FCC (10-100% EtOAc/heptane) to give the compound as a yellow oil (213 mg, 49%). MS (ESI) m/z 185.3 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541432B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-8870ae512a4a46a39d80fff903dd4e74 |
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| Source note | uspto-grants-2013_09 |
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