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 | Dimethylformamide | HCID 6228 | — |
| Product | 1-(triphenylmethyl)-1H-Imidazole-4-acetic acid methyl ester | HCID 10523967 | — |
Reaction Steps
To a solution of methyl 4-imidazoleacetate hydrochloride, as described above in Step A, (4.30 g, 24.3 mmol) in dry DMF (50 mL) were added triethylamine (7.45 mL, 53.5 mmol), then triphenylmethyl bromide (8.64 g, 26.7 mmol). The mixture was stirred at ambient temperature for 18 hours, then partitioned between H2O (250 mL) and EtOAc (250 mL). The organic layer was dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica, eluting with EtOAc, to yield the product as a pale solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06441017B1 |
| Source dataset | uspto-grants-2002_08 |
| ORD ID | ord-797c492c52f74987a2af259a3cf321f9 |
| Source note | uspto-grants-2002_08 |