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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1635593Generated: October 30, 2026

Potassium Iodide → 2,4-Bis(4-tert-butylphenyl)-6-(2-hydroxy-4-ethoxycarbonylmethoxyphenyl)-1,3,5-triazine

https://huagongshe.com/reaction/1635593

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantEthyl chloroacetateHCID 7751—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Bis(4-tert-butylphenyl)-6-(2,4-dihydroxyphenyl)-1,3,5-triazineHCID 135804504—
SolventAcetoneHCID 180—
Product2,4-Bis(4-tert-butylphenyl)-6-(2-hydroxy-4-ethoxycarbonylmethoxyphenyl)-1,3,5-triazineHCID 13574003975%

Reaction Steps

To a stirred mixture of 14 g of 2,4-bis(4-tert-butylphenyl)-6-(2,4-dihydroxyphenyl)-1,3,5-triazine, 10.8 g of anhydrous potassium carbonate, 0.47 g of potassium iodide, and 90 mL of acetone was added 3.7 mL (4,2 g) of ethyl chloroacetate. The mixture was stirred at reflux for 3 hr, and then cooled to room temperature. The solids were removed by filtration and washed with methylene chloride. The product was crystallized from the combined filtrate, washed with cold acetone, and dried in vacuo to give 12.5 g of 2,4-bis(4-tert-butylphenyl)-6-(2-hydroxy-4-ethoxycarbonylmethoxyphenyl)-1,3,5-triazine as a near white powder. The structure was verified by 1H-NMR spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06509399B2
Source datasetuspto-grants-2003_01
ORD IDord-c6076b7ccf2d4c4dbb6a03373a53e7ae
Source noteuspto-grants-2003_01