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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1075713Generated: October 28, 2026

Acetic Acid → 6-Methoxy-2-naphthaldehyde

https://huagongshe.com/reaction/1075713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantIodineHCID 807—
Reactant2-Bromo-6-methoxynaphthaleneHCID 78786—
ReactantMagnesiumHCID 5462224—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product6-Methoxy-2-naphthaldehydeHCID 76991—

Reaction Steps

To a reactor equipped with a stirrer are charged 10 grams of 2-bromo-6-methoxynaphthalene prepared as in Example 7 hereof, 1.05 grams of magnesium and 35 mL of tetrahydrofuran (THF). The reaction is initiated by addition of a crystal of iodine. After one hour of heating at reflux with stirring, 10 mL of DMF mixed with 10 mL of THF is added and the mixture is again refluxed with stirring for 1.5 hours. The reaction mixture is hydrolyzed by addition of dilute acetic acid and a precipitate of crude 6-methoxy-2-naphthaldehyde is formed. The precipitate is recovered by filtration, washed with water, and purified by crystallization from methanol.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05907069
Source datasetuspto-grants-1999_05
ORD IDord-dcdd0f716b5146b388df8cc2fe2fd992
Source noteuspto-grants-1999_05