HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1067667Generated: October 31, 2026
1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde → HCID 178440796, compound
https://huagongshe.com/reaction/1067667
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde | HCID 618233 | — |
| Reactant | 2-Methylpropan-2-olate | HCID 4574913 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Reactant | 3-Phenylpropyl triphenylphosphonium bromide | HCID 10928647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178440796 | HCID 178440796 | — |
Reaction Steps
10 mmol of 3-phenylpropyltriphenylphosphonium bromide, 10 mmol of (1-triphenylmethyl-1H-imidazol-4-yl)methanal (J. L. Kelley, C. A. Miller, E. W. Mc Lean, J. Med. Chem. 1977, 20, 721) and 12 mmol of potassium of t-butanolate are stirred for 24 hours in 50 ml THF. The solvent is evaporated off under reduced pressure, hydrolysed with water and extracted using chloroform. The concentrated organic extract is heated from reflux in 30 ml 2N HCl and 30 ml of acetone for 1 hour. The solvent is evaporated off under reduced pressure and triphenylmethanol is extracted using diethyl ether. The aqueous phase is alkalized using ammonia and the crude product is extracted using diethyl ether. The aqueous phase is alkalized using diethyl ether and crystallized as hydrogen maleate from diethyl ether and ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06248765B1 |
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| Source dataset | uspto-grants-2001_06 |
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| ORD ID | ord-a4c6ae19dac64578b2008e550852aea2 |
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| Source note | uspto-grants-2001_06 |
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