Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 22916442 | HCID 22916442 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 22916451 | HCID 22916451 | 67% |
Reaction Steps
Boron tribromide (0.7 ml) was added to a suspension of 1-(7-carboxyheptyl)-4,5-bis(4-methoxyphenyl)-2-phenylimidazole (0.7 g) in anhydrous dichloromethane (20 ml ) and the reaction was stirred at room temperature for 1 h. Boron tribromide (0.3 ml) was added and the reaction was stirred at reflux for 2 h and at room temperature for 20 h. Water was carefully added to the cooled reaction mixture and the resulting yellow precipitate was collected. Column chromatography on silica gel eluted with a dichloromethane:methanol gradient and recrystallisation from ethanol and water gave 1-(7-carboxyheptyl)-4,5-bis-(4-hydroxyphenyl)-2-phenylimidazole (0.44 g, 67%) as a cream solid, m.p 135°-7°; Found C, 3.97; H, 6.38; N, 5.98%; C29H30N2O4 requires: C, 74.02; H, 6.42; N, 5.95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05663053 |
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| Source dataset | uspto-grants-1997_09 |
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| ORD ID | ord-35d6dba0189f404c995fe4205e533879 |
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| Source note | uspto-grants-1997_09 |
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