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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295538Generated: October 26, 2026

Ethyl vinyl ether → 6-(1-Ethoxy ethoxy)-2-naphthaldehyde

https://huagongshe.com/reaction/1295538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl vinyl etherHCID 8023—
ReactantBenzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
Reactant6-Hydroxy-2-naphthaldehydeHCID 2764110—
CatalystEthyl vinyl etherHCID 8023—
SolventEthyl AcetateHCID 8857—
Product6-(1-Ethoxy ethoxy)-2-naphthaldehydeHCID 2313575973%

Reaction Steps

In a 500 mL three neck flask, equipped with a magnetic stirrer, an addition funnel, and a reflux condenser, were charged 25 g of HNAL (0.1462 mol) and 300 mL of ethyl acetate. 6-Hydroxy-2-naphthaldeyde was not completely soluble even after 3 h stirring at room temperature. To this was added 3.30 g of PPTS (0.0131 mol) and the solution mixture was heated to 70° C. At this temperature, 21 g of ethyl vinyl ether (0.2912 mol) was added dropwise and the reaction mixture became homogeneous upon addition of a few drops of ethyl vinyl ether. After completion of ethyl vinyl ether addition, the reaction temperature was lowered to room temperature and the reaction mixture was stirred overnight. The crude product was purified by column chromatography (silica gel, CH2Cl2) to yield 26 g of pure 6-(1-ethoxy ethoxy)-2-naphthaldehyde (yield: 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244542B2
Source datasetuspto-grants-2007_07
ORD IDord-52e4dc49d2484689aa1609eaca172ff8
Source noteuspto-grants-2007_07