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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881367Generated: October 26, 2026

3,4-Dimethoxystyrene → HCID 178489978, compound

https://huagongshe.com/reaction/1881367

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-DimethoxystyreneHCID 61400—
ReactantDiisopropylethylamineHCID 81531—
ReactantTris(1,1-dimethylethyl)phosphineHCID 83681—
ReactantHCID 178480083HCID 178480083—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 178489978HCID 17848997866%

Reaction Conditions

Temperature135 °C

Reaction Steps

A flask was charged with 5-(2,4-Bis-benzyloxy-5-bromo-phenyl)-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-ol (290 mg; 0.50 mmol), 3,4-dimethoxystyrene (98 mg; 0.60 mmol), tris(dibenzylideneacetone)dipalladium(0) (11 mg; 0.025 eq.), tris-tert-butylphosphine (10 mg; 0.10 eq.), diisopropylethylamine (77 mg; 0.60 mmol), and dimethylformamide (2 mL). The reaction was heated at 135° C. overnight, and then cooled. The solution was diluted with ethyl acetate (40 mL) and washed with water (3×40 mL). The organic layer was dried with sodium sulfate, evaporated, and purified by column chromatography to give 5-{2,4-bis-benzyloxy-5-[2-(3,4-dimethoxy-phenyl)-vinyl]-phenyl}-4-(1-methyl-1H-indol-5-yl)-4H-[1,2,4]triazol-3-ol (220 mg; 0.33 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318790B2
Source datasetuspto-grants-2012_11
ORD IDord-54a90fa267c84a54930fa5777ea8fac9
Source noteuspto-grants-2012_11