Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 23851Generated: October 26, 2026

M-Cresol → 2-(2-Hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine

https://huagongshe.com/reaction/23851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantM-CresolHCID 342—
Reactant1,2,3-TriazineHCID 123047—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant2-Chloro-4,6-bis(4-phenoxyphenyl)-1,3,5-triazineHCID 22568618—
SolventChlorobenzeneHCID 7964—
Product2-(2-Hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazineHCID 135621950—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 0.9 gm of 2-chloro-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine, 0.24 gm of m-cresol and 0.4 gm AlCl3 in 5 ml chlorobenzene was heated to 70° C. under nitrogen and efficient stirring. After about 4 hr at 70° C., the reaction mixture was analyzed by HPLC, which showed the formation of a new product, and almost disappearance of the starting triazine. The reaction mixture was cooled to room temperature and quenched with water. It was then extracted with methylene chloride, and the organic layer separated, washed with water, dried, and concentrated to give a crude product. The crude product was crystallized from acetone to give almost pure 2-(2-hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazine identified by HPLC, NMR and mass spectroscopy.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855269B2
Source datasetuspto-grants-2005_02
ORD IDord-3c8ad07ec9e243c7b04ad3605668233c
Source noteuspto-grants-2005_02