HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → Ethyl 1-trityl-1H-imidazole-4-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178469898 | HCID 178469898 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | Ethyl 1-trityl-1H-imidazole-4-carboxylate | HCID 618225 | — |
Reaction Steps
A suspension of ethyl imidazole-4-carboxylate (1.4 g), triethylamine (1.2 g) and chloroform (20 ml) was stirred at room temperature while trityl chloride (3.06 g) was added, and the mixture was stirred at room temperature for 1 h. The resulting solution was washed with water, dried and evaporated to dryness under reduced pressure, and the residue was crystallised from a mixture of ethyl acetate and cyclohexane, to give ethyl 1-tritylimidazole-4-carboxylate, mp 163°-164°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE036617 |
| Source dataset | uspto-grants-2000_03 |
| ORD ID | ord-91ce51a165e840c2a0015a804d1ff624 |
| Source note | uspto-grants-2000_03 |