HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → methyl N-triphenylmethyl-5-benzimidazolecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | methyl 1H-benzimidazole-5-carboxylate hydrochloride | HCID 22710297 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl N-triphenylmethyl-5-benzimidazolecarboxylate | HCID 22710354 | 106.7% |
Reaction Steps
In dichloromethane (15 ml), methyl 5-benzimidazolecarboxylate hydrochloride (1.00 g) was suspended. To the resulting suspension, triethylamine (1.50 ml) and triphenylmethyl chloride (1.50 g) were added, followed by stirring at room temperature for 3 hours. The reaction mixture was diluted with dichloromethane, washed with water, and dried over anhydrous sodium sulfate. The residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (hexane:ethyl acetate=2:1), whereby title compound (2.10 g, quant.) was obtained as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06747023B1 |
| Source dataset | uspto-grants-2004_06 |
| ORD ID | ord-af0bf4a0bddb49e6b50c4a70c60ee1ea |
| Source note | uspto-grants-2004_06 |