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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095283Generated: November 1, 2026

2-Iodotoluene → HCID 68940392, compound

https://huagongshe.com/reaction/2095283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-IodotolueneHCID 5128—
ReactantCesium fluorideHCID 25953—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantEthyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylateHCID 16050160—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventMethanolHCID 887—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68940392HCID 68940392—

Reaction Steps

To a mixture of ethyl 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indole-2-carboxylate (Paul et al. J. Am. Chem. Soc. 2006, 128, 15552-15553) (1.6 g), tri-(t-butyl)phosphonium tetrafluoroborate (0.074 g), tris(dibenzylideneacetone)dipalladium(0) (0.116 g) and cesium fluoride (2.313 g) was added ortho-iodotoluene (0.781 ml), then dioxane (200 ml) and methanol (20 ml). The reaction mixture was immediately purged with nitrogen and stirred at room temperature for 2 hours. Additional amounts of (dibenzylideneacetone)dipalladium(0) (0.116 g), ortho-iodotoluene (0.781 ml), CsF (2.313 g), and tri-(t-butyl)phosphonium tetrafluoroborate (0.074 g) were added at the same time. The resulting solution was stirred at room temperature overnight. The insoluble material was filtered off and the filtrate was concentrated and the residue was purified by flash chromatography, eluting with 0-100% dichloromethane in hexane to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445679B2
Source datasetuspto-grants-2013_05
ORD IDord-b59c1fbb46244a71addcf6843423f3bc
Source noteuspto-grants-2013_05