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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 484011Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/484011

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSulfuric AcidHCID 1118—
EduktTrimethylhydroquinoneHCID 12785—
EduktPhenyl(pyridin-3-yl)methanolHCID 234839—
EduktSodium BicarbonateHCID 516892—
Lösungsmittel1,1-DichloroethaneHCID 6365—
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 dichloroethane, 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
PatentnummerUS05229385
Quelldatensatzuspto-grants-1993_07
ORD IDord-ba030d7d5b38469aaeafe5928835ec4c
Quellennotizuspto-grants-1993_07