HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1H-Imidazole-4-carbaldehyde | HCID 76428 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde | HCID 618233 | 67% |
Reaction Steps
Triethylamine (3.05 ml, 21.86 mmol) was added to a solution of 1H-imidazole-4-carbaldehyde (2 g, 20.82 mmol) and triphenylmethyl chloride (5.80 g, 20.82 mmol) in N,N-dimethylformamide (20 ml). The reaction mixture was stirred at room temperature for 18 hours. The crude mixture was concentrated in vacuo and partitioned between ethyl acetate and water. The organic phase was washed dried over sodium sulfate, filtered and concentrated in vacuo. The residue was recrystallised from dichloromethane and hexanes to afford the title compound as a cream solid (4.7 g, 67% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08741931B2 |
| Source dataset | uspto-grants-2014_06 |
| ORD ID | ord-17f731ac6baf44c580e08c51e88315b6 |
| Source note | uspto-grants-2014_06 |