HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → methyl 1-benzyl-1H-1,2,4-triazole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | methyl 1H-1,2,4-triazole-1-carboxylate | HCID 642208 | — |
| Product | methyl 1-benzyl-1H-1,2,4-triazole-3-carboxylate | HCID 67023628 | — |
Reaction Steps
A solution of methyl 1,2,4-triazole-2-carboxylate (6.89 g, 54.2 mmole), benzyl bromide (7.7 mL, 65.0 mmol) and potassium carbonate (11.24 g, 81.3 mmol) in acetonitrile (100 mL) was refluxed overnight. The solution was then filtered and concentrated to a residue. The residue was dissolved in diethyl ether. The solution washed with 1N sodium hydroxide one time and water one time, and then dried over MgSO4. The solution was filtered and concentrated to yield 1-benzyl-1H-[1,2,4]triazole-3-carboxylic acid methyl ester as a brown oil, which was used in next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07531545B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-3f7ccd8f78dc45109610f39641ee36b2 |
| Source note | uspto-grants-2009_05 |