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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1607393Generated: October 31, 2026

1-Naphthaldehyde → HCID 54004068, compound

https://huagongshe.com/reaction/1607393

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantSodium hydrideHCID 24758—
ReactantMonoethyl succinateHCID 70610—
SolventEthanolHCID 702—
ProductHCID 54004068HCID 54004068—

Reaction Steps

To a solution of 8.71 g of succinic acid ethyl ester and 7.81 g of 1-naphthylaldehyde in 50 ml of absolute ethanol was added 3.02 g of a 50% sodium hydride (suspension in oil) under ice-cooling, and then the mixture was heated under reflux for 3 hours. After cooling, the reaction mixture was concentrated under reduced pressure. Water was added to the residue, and the mixture was extracted with diethyl ether to remove neutral materials. The aqueous layer was acidified by adding concentrated hydrochloric acid and extracted with diethyl ether. The ethereal layer was washed with a saturated sodium chloride aqueous solution, and dried over anhydrous magnesium sulfate. The ethereal solution was concentrated under reduced pressure to obtain 11.8 g of 3-ethoxycarbonyl-4-(1-naphthyl-3-butenoic acid as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04863904
Source datasetuspto-grants-1989_09
ORD IDord-fd78333c3c1f464b97e345d38a315e6e
Source noteuspto-grants-1989_09