HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-1,2,4-Triazole → 3,4-Dihydro-2-(1H-1,2,4-triazole-1-yl)1(2H)-Naphthalenone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1(2H)-Naphthalenone, 2-bromo-3,4-dihydro- | HCID 101120 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3,4-Dihydro-2-(1H-1,2,4-triazole-1-yl)1(2H)-Naphthalenone | HCID 14698800 | — |
Reaction Steps
To a mixture of 30 g. potassium carbonate, 15 g. 1,2,4-triazole and 250 ml acetonitrile at 40° C. was added a solution of 45 g. 3,4-dihydro-2-bromo-1(2H)-naphthalenone in 150 ml acetonitrile. The mixture was allowed to react for 5 hours at 40° C. and then at reflux temperature for 2 hours. The solid was removed by filtration and the filtrate concentrated to dryness leaving a solid residue. This was dissolved in dichloromethane and washed twice with water. The organic extract was dried over sodium sulfate and evaporated to give 42 grams of product having a melting point of 96°-98° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05106409 |
| Source dataset | uspto-grants-1992_04 |
| ORD ID | ord-e1e1bfa493a14b22a5c7529749bde115 |
| Source note | uspto-grants-1992_04 |