Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | 2-Fluoro-3-(trifluoromethyl)benzophenone | HCID 2737552 | — |
| Product | HCID 21555860 | HCID 21555860 | 90% |
Reaction Steps
A suspension of (2-fluoro-3-trifluoromethyl-phenyl)-phenyl-methanone (0.5 g, 1.87 mmol) in 10 ml of ammonium hydroxide (28%) was sealed in a heavy-welled Pyrex tube. The sealed tube was heated at 140° C. overnight. The reaction was poured into water/saturated ammonium chloride solution and extracted with ethyl acetate. The combined organics was dried over MgSO4 and concentrated to give (2-amino-3-trifluoromethyl-phenyl)-phenyl-methanone as an oil (0.45 g, 90%). MS ESI (m/z) 266 ([M+H]+);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07700595B2 |
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| Source dataset | uspto-grants-2010_04 |
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| ORD ID | ord-613f98253c564c3ca993aff978fd0223 |
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| Source note | uspto-grants-2010_04 |
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