HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261975Generated: October 25, 2026
Potassium Iodide → 1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanol
https://huagongshe.com/reaction/261975
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Picric Acid | HCID 6954 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | Bis-(4-chloro-phenyl)-(1H-imidazol-2-yl)-methanol | HCID 12433870 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Benzyl-alpha,alpha-bis(p-chlorophenyl)imidazole-2-methanol | HCID 12433938 | — |
Reaction Steps
A solution of 19.2 g of α,α-bis(p-chlorophenyl)imidazole-2-methanol (prepared according to Example III B) and 3 g of sodium hydroxyde in 250 ml. of acetonitrile was refluxed for one hour with stirring. Then 500 mg of picric acid, a few crystals of potassium iodide and a solution of 11.3 g of benzyl bromide in 100 ml. of acetonitrile were added. Refluxing was then continued for 4 hours with stirring. The reaction mixture was kept standing overnight. The precipitate formed was filtered off and dissolved in 3 liter of diethyl ether. This solution was washed with a saturated sodium chloride solution, decolorized with active charcoal, dried over sodium sulphate and concentrated. The residue was crystallised from a mixture of methanol and diethyl ether. 1-Benzyl-α,α-bis(p-chlorophenyl)imidazole-2-methanol was obtained. Melting point 167°-168° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04152441 |
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| Source dataset | uspto-grants-1979_05 |
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| ORD ID | ord-81c13b075a9449d79becd3cecb290bc5 |
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| Source note | uspto-grants-1979_05 |
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