HuagongsheHuagongshe Chemistry Print Report · For research reference only
Cyanuric chloride → 2,4-Dichloro-6-phenyl-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Cyanuric chloride | HCID 7954 | — |
| Reactant | HCID 178420626 | HCID 178420626 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4-Dichloro-6-phenyl-1,3,5-triazine | HCID 15549 | — |
Reaction Steps
(Step 1) To 50 g of 2,4,6-trichloro-1,3,5-triazine was added 300 ml of dry tetrahydrofuran and while the mixture was stirred at room temperature, 150 ml of 2M phenylmagnesium bromide-tetrahydrofuran was added dropwise over about 30 minutes. After completion of dropwise addition, the mixture was stirred at room temperature for 1 hour, and then concentrated. To the residue was added iced water and the resultant was extracted with ether. The extract was washed with water, dried over MgSO4, and concentrated. The resulting crystal crop was recrystallized from isopropyl alcohol to provide 21.1 g of 2,4-dichloro-6-phenyl-1,3,5-triazine as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06191149B1 |
| Source dataset | uspto-grants-2001_02 |
| ORD ID | ord-fa5b09b24dba42f1bbcdaec160dd76b1 |
| Source note | uspto-grants-2001_02 |