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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379540Generated: October 30, 2026

1-Naphthaldehyde → HCID 11264629, compound

https://huagongshe.com/reaction/379540

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantHCID 18366765HCID 18366765—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductHCID 11264629HCID 11264629—

Reaction Steps

220 ml of a 1N solution of potassium tert-butoxide in tetrahyclrofuran are added dropwise to a solution of 0.219 mol of ethoxycarbonyltriphenylphosphonium bromide in 200 ml of tetrahydrofuran. The medium is stirred for 1 h at room temperature, after which a solution of 0.22 mol of naphthalene-1-carboxaldehyde in tetrahydrofuran is added dropwise. The medium is stirred for 4 h at room temperature, filtered, the solvent is evaporated off and the residue is taken up in 400 ml of methylene chloride. The organic phase is washed with 100 ml of water, dried and concentrated. The residue is taken up in diisopropyl ether, the precipitate is filtered off and the expected product is obtained after concentration of the solvent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06300340B1
Source datasetuspto-grants-2001_10
ORD IDord-d281675b471c4f6fbdf0e5aa9b788c92
Source noteuspto-grants-2001_10