HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → Bifonazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | 4-(Chlorophenylmethyl)-1,1'-biphenyl | HCID 111006 | — |
| Reactant | TMS-Imidazole | HCID 14420972 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Bifonazole | HCID 2378 | 52.1% |
Reaction Steps
167 g (0.6 mol) of biphenyl-4-yl-phenyl-chloromethane [alternatively named as diphenyl-phenyl-chloromethane or as α-(biphenyl-4-yl)benzyl chloride] and 92 g (0.66 mol) of trimethylsilylimidazole, dissolved in 500 ml of acetonitrile, are heated under reflux for 15 hours. After distilling off the solvent, the crystalline residue is purified by recrystallization from ethyl acetate. 97 g (52% of theory) of (biphenyl-4-yl)-imidazol-1-yl-phenylmethane of melting point 142° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04118487 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-5bffc8abda5f4c0ba78b60f58d66befa |
| Source note | uspto-grants-1978_10 |