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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2050912Generated: October 27, 2026

Benzyl Chloride → Ethyl 5-Benzyloxy-3-hydroxy-2-naphthoate

https://huagongshe.com/reaction/2050912

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantSodiumHCID 5360545—
ReactantEthyl 3,5-dihydroxynaphthalene-2-carboxylateHCID 14773083—
SolventEthanolHCID 702—
ProductEthyl 5-Benzyloxy-3-hydroxy-2-naphthoateHCID 147730847%

Reaction Steps

To a stirred solution of 7.8 g (0.34 g atom) of sodium in 1,000 cc of ethanol, was added 85 g (0.37 mole) of ethyl 3,5-dihydroxy-2-naphthoate. After one-half hour 47 g (0.37 mole) of benzyl chloride was added. The reaction mixture was warmed under reflux for 24 hours. The hot reaction mixture was filtered and cooled in an ice bath. A tan solid precipitated out, which was filtered off yielding 15.0 g (m.p. 98°-115° C.) of the crude product. Recrystallization first from ethanol and then from acetonitrile furnished ethyl 5-benzyloxy-3-hydroxy-2-naphthoate, m.p. 112°-114° C. in 7 percent yield (7.3 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05015663
Source datasetuspto-grants-1991_05
ORD IDord-191deefae9934f7f92c4754152a056ec
Source noteuspto-grants-1991_05