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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 463328Generated: October 29, 2026

Allyl bromide → Ethyl 7-allyloxynaphthalene-2-carboxylate

https://huagongshe.com/reaction/463328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantEthyl 7-hydroxynaphthalene-2-carboxylateHCID 12635629—
CatalystPotassium IodideHCID 4875—
SolventAcetoneHCID 180—
ProductEthyl 7-allyloxynaphthalene-2-carboxylateHCID 2028295381%

Reaction Steps

A mixture of ethyl 7-hydroxynaphthalene-2-carboxylate (37.5 g), anhydrous potassium carbonate (24.0 g), potassium iodide (0.5 g), and allyl bromide (29.0 g) was heated in refluxing acetone (200 ml) with stirring for 15 hours. The mixture was filtered and the filtrate was evaporated. The residue was dissolved in ethyl-acetate, washed with 2% sodium hydroxide solution and water, dried and evaporated to give a solid. Crystallisation from petroleum ether (b.p. 40-60) afforded ethyl 7-allyloxynaphthalene-2-carboxylate (36 g), m.p. 60°-61°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04518612
Source datasetuspto-grants-1985_05
ORD IDord-010ec888aa54404db7f6eec6f76e531c
Source noteuspto-grants-1985_05