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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 232057Erstellt: 26. Oktober 2026

Sulfuric Acid → 3,5,6-Trimethyl-2-[phenyl-(3-pyridyl)methyl]-1,4-benzoquinone

https://huagongshe.com/reaction/232057

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTrimethylhydroquinoneHCID 12785—
EduktPhenyl(pyridin-3-yl)methanolHCID 234839—
EduktSodium BicarbonateHCID 516892—
LösungsmittelDichloromethaneHCID 6344—
Produkt3,5,6-Trimethyl-2-[phenyl-(3-pyridyl)methyl]-1,4-benzoquinoneHCID 1427776772,9%

Reaktionsschritte

To a solution of 1.0 g (5.4 mmol) of phenyl-(3-pyridyl)methanol and 823 mg (5.4 mmol) of 2,3,5-trimethylhydroquinone in 15 ml of dichloromethane, 0.5 ml (9.4 mmol) of concentrated sulfuric acid was added, and refluxed by heating for 2 hours. The reaction mixture was made weakly alkaline with a saturated aqueous solution of sodium hydrogen carbonate, from which the organic phase was separated while the aqueous phase was extracted with chloroform and the extract was combined with the organic phase. The organic phase was washed with water, dried, and oxidized with air, from which the solvent was evaporated off. The residue was purified with silica gel column chromatography (isopropyl ether-ethyl acetate (1:1)), to give 1.25 g (72.7%) of 3,5,6-trimethyl-2-[phenyl-(3-pyridyl)methyl]-1,4-benzoquinone. The physical data are shown in Table 1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04851413
Quelldatensatzuspto-grants-1989_07
ORD IDord-f09bf5353bec4f68b156e63e3916b353
Quellennotizuspto-grants-1989_07