Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | O-Phenylenediamine | HCID 7243 | — |
| Reactant | 1-[3-(trifluoromethyl)phenyl]propane-1,2-dione | HCID 2777678 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 67199697 | HCID 67199697 | 54% |
Reaction Steps
A mixture of 1,2-phenylenediamine (1.00 g, 9.25 mmol) and 1-[3-(trifluoromethyl)phenyl]propane-1,2-dione (2.00 g, 9.25 mmol) in water (80 mL) was heated at 60° C. overnight, then for 5 h with vigorous stirring. The reaction mixture was allowed to cool to r.t. then acidified with 2N HCl (ca 20 mL) and extracted with EtOAc. The organic phase was washed with brine, dried (MgSO4) and concentrated in vacuo. The residue was triturated with heptane to give the title compound (1.44 g, 54%) as a cream-coloured solid. δH (CDCl3) 8.05-8.16 (m, 2H), 7.96 (s, 1H), 7.85-7.90 (m, 1H), 7.72-7.82 (m, 3H), 7.64-7.71 (m, 1H), 2.79 (s, 3H). LCMS (ES+) 289.3 (M+H)+, RT 4.21 minutes (Method 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399483B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-16cdae4321d84f418651b33d63c88703 |
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| Source note | uspto-grants-2013_03 |
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