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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387318Generated: November 1, 2026

1-Naphthaldehyde → Ethyl 3-(naphthalen-1-yl)prop-2-enoate

https://huagongshe.com/reaction/1387318

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-NaphthaldehydeHCID 6195—
ReactantEthyl acetate hexaneHCID 21226206—
ReactantPotassium tert-butoxideHCID 23665647—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 3-(naphthalen-1-yl)prop-2-enoateHCID 5342857190%

Reaction Steps

22.4 g(0.10 mol) of triethylphosphonoacetate was dissolved in 500 ml of tetrahydrofuran and 12.4 g(1.1 mol) of potassium t-butoxide was slowly added thereto. To this solution was slowly added 15.6 g(0.10 mol) of 1-naphtaldehyde dissolved in 20 ml of tetrahydrofuran and the mixture was stirred for 8 hours. The organic solvent was removed by distillation under reduced pressure. The residue was dissolved in ethyl acetate, washed twice with water, dried over anhydrous magnesium sulfate, concentrated and subjected to column chromatography(eluent: hexane/ethyl acetate=95/5, v/v) to give 20.3 g(0.090 mol, Yield 90%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268363B1
Source datasetuspto-grants-2001_07
ORD IDord-d2d4c5c584074eb287ac9933ae25fd78
Source noteuspto-grants-2001_07