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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232070Generated: October 25, 2026

Water → 1,4-Dimethoxy-3-methylnaphthalene-2-carbaldehyde

https://huagongshe.com/reaction/232070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDimethylformamideHCID 6228—
Reactant2-Bromo-1,4-dimethoxy-3-methylnaphthaleneHCID 292240—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product1,4-Dimethoxy-3-methylnaphthalene-2-carbaldehydeHCID 1284752948.9%

Reaction Steps

A solution of 5.0 g (17.8 mmol) of 2-bromo-1,4-dimethoxy-3-methylnaphthalene in 30 ml of tetrahydrofuran was cooled to -78° C., to which 11.2 ml (17.9 mmol) of 1.6M n-butyllithium hexane solution was added dropwise, and stirred at the same temperature for 10 minutes after completion of the addition. Then 1.3 g (17.8 mmol) of dimethylformamide was added dropwise to the reaction mixture, and stirred at room temperature for 1 hour after completion of the addition. Water was added to the reaction mixture, from which the product was extracted with ethyl acetate. The extract was washed with water, dried, and concentrated. The residue was purified with silica gel column chromatography (hexane-isopropyl ether (8:2)), and crystallized from hexane-isopropyl ether, to give 2.0 g (48.9%) of 2-formyl-1,4-dimethoxy-3-methylnaphthalene. m.p. 95°-96° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851413
Source datasetuspto-grants-1989_07
ORD IDord-190d4df1609b47b6b4466bf078983a7e
Source noteuspto-grants-1989_07