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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 396732Generated: October 26, 2026

N,N-Dimethylbenzylamine → 2-[2-Hydroxy4(3-butoxy-2-hydroxypropyloxy)-phenyl]4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin

https://huagongshe.com/reaction/396732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylbenzylamineHCID 7681—
ReactantButyl glycidyl etherHCID 17049—
Reactant2-(2,4-Dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazineHCID 74276—
SolventO-XyleneHCID 7237—
Product2-[2-Hydroxy4(3-butoxy-2-hydroxypropyloxy)-phenyl]4,6-bis(2,4-dimethylphenyl)-1,3,5-triazinHCID 13560141286%

Reaction Steps

23.8 g (0.06 mol) of 2-(2,4-dihydroxyphenyl)-4,6-bis-(2,4-dimethylphenyl)-1,3,5-triazine (prepared as described in U.S. Pat. No. 3,244,708 Example 16) are suspended in 300 ml of xylene. 12.1 g (0.09 mol) of 97% butyl glycidyl ether and 0.75 g (0.006 mol) of dimethylbenzylamine are added to this suspension, and the mixture is heated to reflux temperature. After a reaction time of 5 hours the clear, brownish solution is cooled and clarified by filtration through 100 g of silica gel. The yellow solution is evaporated and the residue is recrystallized from hexane/toluene. This gives 27.3 g of pale yellow crystals of 2-[2-hydroxy-4(3-butoxy-2-hydroxypropyloxy)-phenyl]-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin (=86% yield). Melting point: 80-83° C. (Compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608122B1
Source datasetuspto-grants-2003_08
ORD IDord-89f6527309c7417da998df8ccd1ab7c7
Source noteuspto-grants-2003_08