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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1066444Erstellt: 26. Oktober 2026

Hydrochloric Acid → 2-(2,4-Dihydroxyphenyl)-4,6-diphenyl-1,3,5-triazine

https://huagongshe.com/reaction/1066444

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktResorcinolHCID 5054—
Edukt2-Chloro-4,6-diphenyl-1,3,5-triazineHCID 19698—
EduktSodium MethoxideHCID 10942334—
LösungsmittelMethanolHCID 887—
LösungsmittelO-XyleneHCID 7237—
LösungsmittelSulfolaneHCID 31347—
Produkt2-(2,4-Dihydroxyphenyl)-4,6-diphenyl-1,3,5-triazineHCID 135437125—

Reaktionsbedingungen

Temperatur118 °C

Reaktionsschritte

A 500 mL three-necked, round-bottomed flask equipped with a mechanical stirrer is charged with 60 g of xylene and 55.5 g (0.207) of 4,6-diphenyl-2-chloro-s-triazine. The mixture is warmed to 118° C. and the pressure is reduced to 300 mbar and 2.8 g of hydrogen chloride gas is charged to the system. The mixture is cooled to 80° C. and a solution of resorcinol (88.2 g, 0.802 mol) in 60 g of tetramethylene sulfone is added dropwise over a 7-minute period. The mixture is stirred at 80° C. for six hours and then for one hour at 100° C. The temperature is reduced to 60° C. and a 300 mL portion of methanol is added. The mixture is allowed to cool to room temperature and is stirred overnight. Sodium methoxide (41.3 g) is added portionwise to adjust the pH to 5.0-5.5. The solids are collected by vacuum filtration and are washed with methanol and water. After drying, the title compound is obtained in a yield of 59.2 g as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06242598B1
Quelldatensatzuspto-grants-2001_06
ORD IDord-b4fb05a14f424cdcbcd193bd5795b8a8
Quellennotizuspto-grants-2001_06