HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-[(5-Formylimidazol-1-yl)methyl]benzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(4-Cyanobenzyl)-5-hydroxymethyl-1H-imidazole | HCID 10198247 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 4-[(5-Formylimidazol-1-yl)methyl]benzonitrile | HCID 10632289 | — |
Reaction Steps
To a solution of the alcohol from Step D (21.5 g, 101 mol) in DMSO (500 ml) at room temperature was added triethylamine 56 ml, 402 mmol), then SO3 -pyridine complex (40.5 g, 254 mmol). After 45 min, the reaction was poured into EtOAc, washed with water and brine, dried (Na2SO4), and concentrated in vacuo to provide the aldehyde as a white powder which was sufficiently pure without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05891889 |
| Source dataset | uspto-grants-1999_04 |
| ORD ID | ord-b5eea04c267b42069af37b45fdb8d6df |
| Source note | uspto-grants-1999_04 |