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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 277629Erstellt: 24. Oktober 2026

Benzoyl chloride → 4-Benzoyloxy-2-methylnaphthol

https://huagongshe.com/de/reaction/277629

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktBenzoyl chlorideHCID 7412—
EduktMenadiolHCID 10209—
LösungsmittelPyridineHCID 1049—
Produkt4-Benzoyloxy-2-methylnaphtholHCID 2262540969,3%

Reaktionsschritte

9.7 g (0.056 mol) of 2-methyl-1,4-dihydroxynaphthalene was dissolved in 60 ml of pyridine, and, while stirring under ice-cooling, 8.4 g (0.06 mol) of benzoyl chloride was added dropwise. Following completion of the addition, stirring was continued under ice-cooling for 30 minutes, and for further one hour at room temperature. The reaction mixture was concentrated under reduced pressure, the residual oil extracted with ethyl acetate, washed with 1N HCl and then water, and the organic layer concentrated under reduced pressure. Methanol was added to the residue, the precipitated crystals collected by filtration and recrystallized from methanol to give 10.8 g of white crystals, m.p. 172-174° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06358515B2
Quelldatensatzuspto-grants-2002_03
ORD IDord-91770afe4a5f4c058ae10ae9f130275c
Quellennotizuspto-grants-2002_03