Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bifonazole | HCID 2378 | — |
| Reactant | 2-Chlorotrityl chloride | HCID 94524 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86737425 | HCID 86737425 | 83.4% |
Reaction Steps
15.1 g (0.05 mol) of 1-[α-(4-biphenylyl)-benzyl]-imidazole and 15.2 g (0.05 mol) of 2-chlorophenyl-diphenylmethyl chloride are suspended in 400 ml of acetonitrile and the suspension is heated to 80° C. for 24 hours. It is then filtered and the filtrate is concentrated by distilling off the solvent. The residue crystallises after trituration with ether. 13 g (42% of theory) of 1-[α-(4-biphenylyl)-benzyl]-3-(2-chlorophenyl-diphenyl-methyl)-imidazolium chloride of melting point 140° C. (with decomposition) are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04243670 |
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| Source dataset | uspto-grants-1981_01 |
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| ORD ID | ord-b577c5edf68d460d90d7a444b920bcd4 |
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| Source note | uspto-grants-1981_01 |
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