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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2293005Generated: October 29, 2026

Butyl glycidyl ether → HCID 135828183, compound

https://huagongshe.com/reaction/2293005

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl glycidyl etherHCID 17049—
ReactantHCID 135845402HCID 135845402—
CatalystPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
SolventMesityleneHCID 7947—
SolventEthyl AcetateHCID 8857—
ProductHCID 135828183HCID 135828183104.8%

Reaction Conditions

Temperature140 °C

Reaction Steps

A mixture of 20.0 g (0.048 mol) of 2-mesityl-4,6-bis(2,4-dihydroxyphenyl)-1,3,5-triazine (compound 1b), 13.8 g (0.105 mol) of n-butyl glycidyl ether (purity 95%) and 1.8 g (4.8 mmol) of ethyltriphenylphosphonium bromide (purity 97%) in 100 ml of mesitylene (purity 99%) is stirred at 140° C. under nitrogen for 21 hours. Decantation and evaporation of the remaining solvent gives 41.2 g of crude product. This is dissolved in 100 ml of ethyl acetate and filtered through a 10.5 cm layer of silica gel 60 (230-400 mesh) of diameter 7.5 cm, with elution with 3 l of ethyl acetate/hexane (1:1 mixture). The 34.0 g of solid obtained after removal of the solvent are re-dissolved in 25 ml of ethyl acetate. 250 ml of hexane are added to the viscous solution. The mixture is stirred at 0° C. for 2 hours and filtered, and the solid is dried for 24 hours at 80° C. and a pressure of 60 mmHg (8000 Pa), giving 23.0 g of the title product (compound 2) of the formula ##STR105## of m.p. 125°-131° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05686233
Source datasetuspto-grants-1997_11
ORD IDord-24065dd9fa8c442697abdfd7101f5951
Source noteuspto-grants-1997_11