HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroform → 3-Chloro-6-(o-fluorophenyl)-1,2,4-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-(o-fluorophenyl)-1,2,4-triazin-3(2H)-one | HCID 12581286 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 3-Chloro-6-(o-fluorophenyl)-1,2,4-triazine | HCID 21315222 | — |
Reaction Steps
A suspension of 42.4 g. of 6-(o-fluorophenyl)-1,2,4-triazin-3(2H)-one in 350 ml. of chloroform is refluxed overnight, cooled in an ice bath, and 350 ml. of phosphorus oxychloride followed by 2.6 g. of N,N-dimethylformamide are added. The mixture is refluxed for 4.5 hours, cooled and concentrated to a brown oil. This oil is dissolved in methylene chloride, poured onto ice and made basic, giving a brown solid. The mixture is filtered and the filtrate is passed through a silica gel column giving a crystalline solid. This solid is heated with hexane and filtered giving crystals. Recrystallization from hexane gives a tan solid which sublimes on heating giving 3-chloro-6-(o-fluorophenyl)-1,2,4-triazine as tan crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04159375 |
| Source dataset | uspto-grants-1979_06 |
| ORD ID | ord-98ef7605ac974f9aba1b45a37003067e |
| Source note | uspto-grants-1979_06 |