Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 3-Aminophenol | HCID 11568 | — |
| Reactant | Benzophenone imine | HCID 136809 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(Benzhydrylidene-amino)-phenol | HCID 21877269 | — |
Reaction Steps
3-(Benzhydrylidene-amino)-phenol was prepared as follows: A stirred solution of benzophenone imine (15.0 g, 82.8 mmol) and 3-aminophenol (9.03 g, 82.8 mmol) in 25 mL toluene was heated at reflux with removal of H2O with a Dean-Stark trap for 3.5 h. The crystals that formed from the cooled reaction mixture were collected by vacuum filtration, washed with hexanes and air dried. In this manner, 3-(benzhydrylidene-amino)phenol was obtained as a light yellow solid (17.3 g, 76%): 1H NMR (CDCl3) & 7.64 (d, 2H, J=7.1 Hz), 7.38 (d, 1H, J=7.1 Hz), 7.34-7.15 (m, 7H), 7.04 (d, 2H, J=7.2 Hz), 6.88 (t, 1H, J=8.1 Hz), 6.82 (d, 1H, J=8.2 Hz), 6.23 (s, 1H), 6.21 (d, 1H, J=7.8 Hz). Anal. Calc. for C19H15NO: C, 83.49; H, 5.53; N, 5.12. Found: C, 83.51; H, 5.65; N, 5.03.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06884890B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-9cff83f9a4224630bdf2c12b4fb93803 |
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| Source note | uspto-grants-2005_04 |
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