HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trityl chloride → 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trityl chloride | HCID 6456 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178418812 | HCID 178418812 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester | HCID 10523967 | 104% |
Reaction Steps
A solution of the product from Step 4.a. (3.2 g, 17.5 mmol) in DMF (50 ml) was treated with chlorotriphenylmethane (4.88 g, 17.5 mmol) and Et3N (5.4 ml, 38.5 mmol) and the reaction was stirred at room temperature for about 6 hours. The DMF was evaporated under reduced pressure and the residue was distributed between EtOAc and saturated NaCl solution. The EtOAc layer was dried over Na2SO4, filtered and concentrated under reduced pressure to yield product as a viscous oil (6.96 g, 104%) which crystallized on standing. Mass spec. 383.3 MH+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084135B1 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-f14b9450f13e42b58be4c562d609b698 |
| Source note | uspto-grants-2006_08 |