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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277650Erstellt: 24. Oktober 2026

Methylhydroquinone → 4-Benzoyloxy-2-methylphenol

https://huagongshe.com/de/reaction/277650

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylhydroquinoneHCID 7253—
EduktBenzoyl chlorideHCID 7412—
Produkt4-Benzoyloxy-2-methylphenolHCID 1465033068,2%

Reaktionsschritte

Using 5.0 g of methylhydroquinone and 5.6 g of benzoyl chloride, the procedure of Reference Example was followed. Recrystallization from ethanol-isopropyl ether gave 6.2 g of 4-benzoyloxy-2-methylphenol as white crystals, m.p. 120-122. Then, using 6.2 g of thus obtained white crystals, 5.1 g of benzyl bromide and 4.1 g of anhydrous potassium carbonate, the procedure of Reference Example was followed to give 7.6 g of 1-benzyloxy-2-methyl-4-benzoyloxybenzene as white crystals, m.p. 118-119° C. Then, using 7.6 g of thus obtained white crystals, 15 ml of 2N NaOH and 100 ml of methanol, the procedure of Reference Example was followed to give 3.8 g of 4-benzyloxy-3-methylphenol as white crystals, m.p. 70-71° C. Then, using 2.1 g of thus obtained white crystals, 1.4 g of anhydrous potassium carbonate, 4.6 g of chloromethyloxirane and 1.9 g of 1-(2-methoxyphenyl)piperazine, the procedures of Examples 1-A and 2 were followed. Recrystallization from methanol-ethyl acetate gave 3.0 g of white crystals, m.p. 214-216° C. (decomp.).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358515B2
Quelldatensatzuspto-grants-2002_03
ORD IDord-6b00fa4521564013894a818b385466b3
Quellennotizuspto-grants-2002_03