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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23851Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/23851

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktM-CresolHCID 342—
Edukt1,2,3-TriazineHCID 123047—
EduktAluminum(III) ChlorideHCID 6451240—
Edukt2-Chloro-4,6-bis(4-phenoxyphenyl)-1,3,5-triazineHCID 22568618—
LösungsmittelChlorobenzeneHCID 7964—
Produkt2-(2-Hydroxy-4-methylphenyl)-4,6-bis(4-phenoxyphenyl)-1,3,5-triazineHCID 135621950—

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06855269B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-3c8ad07ec9e243c7b04ad3605668233c
Quellennotizuspto-grants-2005_02