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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373106Generated: November 1, 2026

Pempidine → Ethyl 1-naphthylpropiolate

https://huagongshe.com/reaction/2373106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPempidineHCID 6603—
ReactantEthyl chloroformateHCID 10928—
Reactant1-EthynylnaphthaleneHCID 123357—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
CatalystHCID 178418397HCID 178418397—
SolventAcetonitrileHCID 6342—
ProductEthyl 1-naphthylpropiolateHCID 1319356836%

Reaction Steps

First, ethyl 1-naphthylpropiolate was prepared. A mixture of 1-ethynylnaphthalene (7.7 g, 50.6 mmol), 4-(dimethylamino)pyridine (0.06 g, 0.5 mmol), 1,2,2,6,6-pentamethylpiperidine (8.8 g, 55.7 mmol), and acetonitrile (120 mL) was sparged with nitrogen for 10 min, and then tetrakis(triphenylphosphine)palladium(0) (1.3 g, 1.1 mmol) was added. The mixture was sparged with nitrogen for 10 min, heated to reflux, treated dropwise with ethyl chloroformate (12.1 g, 111.3 mmol), and held at reflux for 2 h. The reaction mixture was cooled to ambient and diluted with ligroin. The solution was washed three times with water and then with brine, dried (Na2SO4), and concentrated to deposit a brown oil. The crude product was purified by column chromatography to provide 4.0 g (36% of theory) of ethyl 1-naphthylpropiolate. 1H NMR (CDCl3): δ 1.40 (t, 3H), 4.33 (q, 2H), 7.50 (m, 3H), 7.90 (m, 3H), 8.30 (d, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459263B2
Source datasetuspto-grants-2008_12
ORD IDord-7d7baf9b9b4d48e8b44aa9db32d7bd5f
Source noteuspto-grants-2008_12