Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Cornforth reagent | HCID 2724130 | — |
| Reactant | HCID 19778391 | HCID 19778391 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 19778369 | HCID 19778369 | — |
Reaction Steps
Pyridinium dichromate (7.5 g) was added, with stirring, to a solution of crude [2-(2,6-dichloro-4-trifluoromethylphenyl)-5-methyl-2H-1,2,3-triazol-4-yl]methanol (4.3 g) in dichloromethane (50 ml) at room temperature. The mixture was stirred overnight and then ether (100 ml) and silica (4 g) was added. After 10 minutes, the mixture was filtered through a pad of magnesium sulphate and the solvent was evaporated to give 2-(2,6-dichloro-4-trifluoromethylphenyl]-5-methyl-2H-1,2,3-triazole-4-carboxaldehyde, as a crude brown solid. This product was then treated in similar manner to Example 1 with diaminomaleonitrile to give 2-(2,6-dichloro-4-trifluoromethylphenyl)-4-[(2-amino-1,2-dicyanoethenylimino))methyl]-5-methyl-2H-1,2,3-triazole, m.p. 238°-239°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05109012 |
|---|
| Source dataset | uspto-grants-1992_04 |
|---|
| ORD ID | ord-301abf77485046abb4fce8c77becfe39 |
|---|
| Source note | uspto-grants-1992_04 |
|---|