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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232896Generated: October 30, 2026

Potassium Iodide → 2-(2-Hydroxy-4-hexyloxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazine

https://huagongshe.com/reaction/232896

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant1-BromohexaneHCID 8101—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2,4-Dihydroxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazineHCID 135532479—
SolventGlycol monoethyl etherHCID 8076—
Product2-(2-Hydroxy-4-hexyloxyphenyl)-4,6-bis(4-methoxyphenyl)-1,3,5-triazineHCID 135576267—

Reaction Conditions

Temperature110 °C

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 in 100 ml of 2-ethoxyethanol at 110° C. for 45 minutes, followed by dropwise addition of 6.9 g (0.042 mol) of 1-bromohexane over a period 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 and then washed with methanol and dried. After recrystallization from 2-ethoxyethanol, the pure light yellow product of the formula ##STR23## is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05591850
Source datasetuspto-grants-1997_01
ORD IDord-12b898bd83d946648c9f8711bbb3c7e8
Source noteuspto-grants-1997_01