Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2393838Generated: October 31, 2026

1-Pentyne → Ethyl 4-[(7,8-dihydro-8,8-dimethyl-5-(1-pentynyl)naphth-3-yl)ethynyl]benzoate

https://huagongshe.com/reaction/2393838

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PentyneHCID 12309—
Reactant4-[2-[5,6-Dihydro-5,5-dimethyl-8-[[(trifluoromethyl)sulfonyl]oxy]-2-naphthalenyl]ethynyl]benzoic acid ethyl esterHCID 12017638—
CatalystHCID 178418476HCID 178418476—
SolventDiethylamineHCID 8021—
SolventEthyl AcetateHCID 8857—
ProductEthyl 4-[(7,8-dihydro-8,8-dimethyl-5-(1-pentynyl)naphth-3-yl)ethynyl]benzoateHCID 18314569—

Reaction Conditions

Temperature70 °C

Reaction Steps

A solution (flushed with argon) of 201.3 mg (0.42 mmol) of ethyl 4-[(5-trifluoromethylsulfonyloxy-7,8-dihydro-8,8-dimethylnaphth-3-yl)ethynyl]benzoate (Compound 66), 286.5 mg (4.21 mmol) of 1-pentyne, 59.5 mg (0.08 mmol) of bis(triphenylphosphine)palladium(II) chloride and 32.0 mg (0.17 mmol) of cuprous iodide in 2.5 ml of diethylamine was heated to 70° C. in a pressure vial for 6 hours. After stirring overnight at room temperature, the mixture was diluted with EtOAc (25 ml) and washed with water and brine. The organic phase was dried over MgSO4, concentrated in vacuo and purified by column chromatography (silica, 5% Et2 O-hexanes) to give the title compound as a colorless, air-sensitive oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05808083
Source datasetuspto-grants-1998_09
ORD IDord-702d87562aa2470fbaca5ddbb85aa33c
Source noteuspto-grants-1998_09