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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 324239Generated: October 28, 2026

Diethyl Ether → HCID 22323716, compound

https://huagongshe.com/reaction/324239

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantTriphenylphosphineHCID 11776—
ReactantEthyl 4-iodobenzoateHCID 142891—
ReactantHCID 22323714HCID 22323714—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418476HCID 178418476—
SolventTriethylamineHCID 8471—
ProductHCID 22323716HCID 22323716—

Reaction Steps

A solution of 280.0 mg (1.520 mmol) 6-ethynyl-2,3-dihydro-3,3-dimethyl-1H-inden-1-one (Compound DD) and 419.6 mg (1.520 mmol) ethyl 4-iodobenzoate in 5 ml Et3N was sparged with argon for 40 minutes. To this solution was added 271.0 mg (1.033 mmol) of triphenylphosphine, 53.5 mg (0.281 mmol) of copper(I) iodide, and 53.5 mg (0.076 mmol) of bis(triphenylphosphine)palladium(II) chloride. The resulting mixture was heated to reflux for 2.5 hours, cooled to room temperature, and diluted with Et2O. After filtration through a pad of Celite, the filtrate was washed with H2O, 1 M HCl, H2O, and saturated aqueous NaCl, then dried over MgSO4, and concentrated under reduced pressure. The title compound was isolated as a pale-yellow solid by column chromatography (15% EtOAc-hexanes). 1H NMR (300 MHz, d6-acetone): δ 8.05 (2H, d, J=8.6 Hz), 7.87 (1H, dd, J=1.4, 8.1 Hz), 7.75 (2H, m), 7.70 (2H, d, J=8.5 Hz), 4.36 (2H, q, J=7.1 Hz), 2.60 (2H, s), 1.45 (6H, s), 1.37 (3H, t, J=7.1 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06218128B1
Source datasetuspto-grants-2001_04
ORD IDord-e11743b3bc924be6a2df07ccf3e386b5
Source noteuspto-grants-2001_04