HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromotriphenylmethane | HCID 11692 | — |
| Reactant | HCID 178499561 | HCID 178499561 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester | HCID 10523967 | — |
Reaction Steps
To a solution of the product from Step A (24.85 g, 0.141 mol) in DMF (115 mL) was added triethylamine (57.2 mL, 0.412 mol) and triphenylmethyl bromide (55.3 g, 0.171 mol) and the suspension was stirred for 24 hours. After this time, the reaction mixture was diluted with EtOAc and water. The organic phase was washed with sat. aq. NaHCO3, dried, (Na2SO4) and the solvent evaporated in vacuo. The residue was purified by chromatography (Silica gel, 0-100% EtOAc in hexanes) to provide the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05874452 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-08c666511e2d4ffbb412faa15f71c50c |
| Source note | uspto-grants-1999_02 |