HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenol → 2,4-Dichloro-6-phenoxy-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenol | HCID 996 | — |
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2,4-Dichloro-6-phenoxy-1,3,5-triazine | HCID 20807 | 45% |
Reaction Steps
2,4-Dichloro-6-phenoxy-s-triazine (C) was prepared in 45% yield via the condensation of one equivalent of phenol with cyanuric chloride in chloroform at 50° which also contained one equivalent of sodium hydroxide. The product C, obtained as a white crystalline solid (mp. 110°-112°), was condensed in a second step with B in a manner similar to that described in Example 6. During the course of the reaction a solid appeared which was filtered, air-dried and identified as 7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04128559 |
| Source dataset | uspto-grants-1978_12 |
| ORD ID | ord-ec1a8cd381d3457c93eb6d7b032b695c |
| Source note | uspto-grants-1978_12 |