HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 4-(2-bromophenyl)-1-trityl-1H-imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178419371 | HCID 178419371 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(2-bromophenyl)-1-trityl-1H-imidazole | HCID 22185143 | — |
Reaction Steps
To a solution of crude 4-(2-bromo-phenyl)-1H-imidazole (73.5 g, 0.33 mol) and triethylamine (45.8 ml, 0.33 mol) in dry dimethylformamide (750 ml) at 0° C. was added a solution of trityl chloride in dry dimethylformamide (850 ml) dropwise over 40 min. When the addition was complete, the ice bath was removed and the reaction was stirred at room temperature for 1.5 h. Then the reaction mixture was poured into a stirring mixture of ice water (ca. 2.0 L). A light orange solid precipitated. After stirring for 20 min the solid was filtered and dried to give a light amber solid. This solid was used in the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07026324B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-e3cf39a8b6f3418d8ab8893de9ee70f4 |
| Source note | uspto-grants-2006_04 |