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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855116Generated: October 28, 2026

Ethynylpyridine → HCID 86599493, compound

https://huagongshe.com/reaction/855116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthynylpyridineHCID 137268—
Reactantethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylateHCID 86599457—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418807HCID 178418807—
SolventTolueneHCID 1140—
ProductHCID 86599493HCID 8659949377%

Reaction Steps

A mixture of ethyl 8-iodo-6-(trifluoromethoxy)-2-(trifluoromethyl)-2H-chromene-3-carboxylate prepared as in Example 21a, Step 2 (1.00 g, 2.07 mmole), 2-pyridylacetylene (419 uL, 4.15 mmole), CuI (39 mg, 0.207 mmole), PdCl2(dppf)2-CH2Cl2 (169 mg, 0.207 mmole) and TEA (0.866 mL, 6.21 mmole) in anhydrous toluene (10 mL) was stirred at room temperature for 5 days under a N2 atmosphere. The mixture was then diluted with hexanes and purified by silica chromatography (0% to 75% EtOAc:hexanes gradient) to give 0.73 g (77% yield) the title product as a pale yellow crystalline solid: ESHRMS m/z 458.0849 (M+H, C21H14F6NO4, Calc'd 458.0822).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259266B2
Source datasetuspto-grants-2007_08
ORD IDord-a845c58339c643d3b9f56784ba1f5ba5
Source noteuspto-grants-2007_08