HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Diethyl 1-methyl-2-(methylthio)-1H-imidazole-4,5-dicarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diazomethane | HCID 9550 | — |
| Reactant | Diethyl 2-(methylsulfanyl)-1H-imidazole-4,5-dicarboxylate | HCID 14416595 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | Diethyl 1-methyl-2-(methylthio)-1H-imidazole-4,5-dicarboxylate | HCID 303834 | 97% |
Reaction Steps
The diethyl 2-(methylthio)-4,5-imidazoledicarboxylate (10 g; 0.039 mol) was slowly added in small portions to a solution of diazomethane in ether (containing approximately 3 g of diazomethane). Nitrogen was evolved immediately and the solution was allowed to stand at room temperature overnight. Excess diazomethane was then decomposed by the addition of dilute acetic acid and the reaction mixture was worked up in the usual way. Diethyl 1-methyl-2-(methylthio)-4,5-imidazoledicarboxylate (10.2 g; 97%) was obtained as a thick yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05329012 |
| Source dataset | uspto-grants-1994_07 |
| ORD ID | ord-8b1cfeabcd9342b88f2974a803d4ff71 |
| Source note | uspto-grants-1994_07 |