Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | [2,6-Dichloro-4-(trifluoromethyl)phenyl]hydrazine | HCID 688223 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21188133 | HCID 21188133 | — |
Reaction Steps
A solution of 2,6-dichloro-4-trifluoromethylphenylhydrazine (0.245 g) in ethanol (2 ml) was added to benzoylacetonotrile (0. 145 g) in ethanol (8 ml) and the solution heated at 80° C. for 6 hours. Glacial acetic acid (1 ml) was added and the mixture heated at 80° C. for 4 hours and then 90° C. for 2 hours. The reaction mixture was evaporated and the residue purified by column chromatography on silica gel (10 g) eluted with dichloromethane. Combination and evaporation of appropriate fractions followed by further purification of their residue by reverse phase high performance liquid chromatography on C18 silica eluted with methanol: acetonitrile: water (1:5:4). Combination and evaporation of appropriate fractions gave the title compound as a white solid m.p. 141.5-142.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06255333B1 |
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| Source dataset | uspto-grants-2001_07 |
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| ORD ID | ord-634a5296aa8d405480934285bad699c8 |
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| Source note | uspto-grants-2001_07 |
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