HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-Chloro-3-(2,6-difluorophenyl)-[1,2,4]triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 3-(2,6-difluorophenyl)-[1,2,4]triazin-6(1H)-one | HCID 22727019 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 6-Chloro-3-(2,6-difluorophenyl)-[1,2,4]triazine | HCID 22727021 | — |
Reaction Steps
1 g of 3-(2,6-difluorophenyl)-[1,2,4]triazin-6(1H)-one is placed in 20 ml of dioxane and at room temperature 0.73 g of POCl3 is added. Then, within a period of 5 min, 0.48 g of triethylamine in 3 ml of dioxane is added dropwise and stirring is carried out at room temperature for 30 min. The reaction mixture is then poured into ice-water and extracted with ethyl acetate, and the organic phase is separated off and concentrated. In this way 6-chloro-3-(2,6-difluorophenyl)-[1,2,4]triazine is obtained in the form of a yellow oil. The crude product is reacted further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06723720B2 |
| Source dataset | uspto-grants-2004_04 |
| ORD ID | ord-52dd45e26af841d19b4dd7ea3e589ce2 |
| Source note | uspto-grants-2004_04 |