Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277629Generated: October 26, 2026

Benzoyl chloride → 4-Benzoyloxy-2-methylnaphthol

https://huagongshe.com/reaction/277629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantMenadiolHCID 10209—
SolventPyridineHCID 1049—
Product4-Benzoyloxy-2-methylnaphtholHCID 2262540969.3%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06358515B2
Source datasetuspto-grants-2002_03
ORD IDord-91770afe4a5f4c058ae10ae9f130275c
Source noteuspto-grants-2002_03