HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 2-(2-Hydroxy-4-hexyloxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 1-Bromohexane | HCID 8101 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(2,4-Dihydroxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazine | HCID 135532479 | — |
| Solvent | Glycol monoethyl ether | HCID 8076 | — |
| Product | 2-(2-Hydroxy-4-hexyloxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazine | HCID 135576267 | — |
Reaction Steps
15.2 g (0.038 mol) of 2-(2,4-dihydroxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazine of the formula (108b), 5.2 g of potassium carbonate and 50 mg of potassium iodide are heated at 110 C. in 100 ml of 2-ethoxyethanol for 45 minutes, and then 6.9 g (0.042 mol) of 1-bromohexane are added dropwise over the course of 15 minutes. The mixture is stirred at 110 C. for 12 hours, cooled to 0 C. and filtered. The solid material is washed neutral with water, then washed with methanol and dried. Recrystallization from 2-ethoxyethanol gives the pure, light-yellow product of the formula ##STR23##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05688995 |
| Source dataset | uspto-grants-1997_11 |
| ORD ID | ord-c511b1acb53e450f91b9618f3c608591 |
| Source note | uspto-grants-1997_11 |