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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 488116Generated: October 29, 2026

Water → 5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehyde

https://huagongshe.com/reaction/488116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantSodium hydrideHCID 24758—
Reactant5-Ethyl-4-hydroxy-3-methoxy-1-naphthalenecarbaldehydeHCID 10263239—
SolventDimethylformamideHCID 6228—
Product5-Ethyl-3-methoxy-4-methoxymethoxy-1-naphthalenecarbaldehydeHCID 9970569—

Reaction Steps

324 g of 5-ethyl-4-hydroxy-3-methoxy-1-naphthalenecarbaldehyde was dissolved in 1 liter of N,N-dimethylformaldehyde, to which 68 g of 60% sodium hydride was gently added under ice-cooling conditions. After agitation for 10 minutes, 128 ml of chloromethyl methyl ether was gradually added so that the reaction temperature did not exceed 15° C. After agitation at room temperature for 20 minutes, the reaction solution was poured into iced water and extracted with ethyl acetate. The resultant organic phase was washed with a saturated saline solution and dried with anhydrous magnesium sulfate. The solvent was distilled off and the resultant residue was purified by silica gel column chromatography (5% ethyl acetate/hexane) to obtain 288 g of the captioned compound as a brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05298649
Source datasetuspto-grants-1994_03
ORD IDord-1425fbee7f1f455f91ce2dd4b60c680e
Source noteuspto-grants-1994_03