Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | HCID 178440152 | HCID 178440152 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178440153 | HCID 178440153 | 50% |
Reaction Steps
To a suspension of 4-(1-methylethyl)-5-phenyl-α,α-bis(trifluoromethyl)-1H-imidazole-2-methanol (1.75 g) in 40 ml of water was added 2.5 ml of concentrated nitric acid in a dropwise manner. The mixture was stirred for 30 minutes, and the nitrate salt, 1.51 g) was filtered off. The solid in 5 ml of concentrated sulfuric acid was heated at reflux for 2 hours. The reaction mixture was poured into 50 ml of ice-water. The mixture was basified to a pH of 8 and extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to dryness to afford a yellow solid which was purified by flash chromatography on silica gel (85:15 hexane/ethyl acetate) to afford (0.98 g, 50%) of the title compound as a pale yellow solid, m.p. 157°-160° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04632930 |
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| Source dataset | uspto-grants-1986_12 |
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| ORD ID | ord-4e8344c5b8954a1ab8bf76d9d1fd3574 |
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| Source note | uspto-grants-1986_12 |
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