Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 403682Generated: October 29, 2026

N,N'-Dimethylethylenediamine → 1-(3-tert-butyl-5-iodo-4-methoxyphenyl)pyridin-2(1H)-one

https://huagongshe.com/reaction/403682

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N'-DimethylethylenediamineHCID 8070—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1-(Tert-butyl)-3,5-diiodo-2-methoxybenzeneHCID 57419440—
ReactantHCID 178516071HCID 178516071—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product1-(3-tert-butyl-5-iodo-4-methoxyphenyl)pyridin-2(1H)-oneHCID 66833852—

Reaction Conditions

Temperature110 °C

Reaction Steps

In a 20 mL microwave tube were added pyridin-2-ol (190 mg, 2 mmol), copper(I) iodide (76 mg, 0.400 mmol), 1-tert-butyl-3,5-diiodo-2-methoxybenzene (998 mg, 2.400 mmol), potassium phosphate (849 mg, 4.00 mmol) and N,N′-dimethylethylenediamine (0.086 mL, 0.800 mmol) in dioxane (10 mL). The tube was sealed and the mixture was sparged with N2 for 10 minutes and heated in an oil bath at 110° C. for 16 hours. The mixture was cooled and partitioned into ethyl acetate. The organic layer was washed with saturated NaHCO3, brine, dried (Na2SO4), filtered and the filtrate was treated with 3-mercaptopropyl functionalized silica gel, filtered through diatomaceous earth and concentrated in vacuo to give crude product which was purified on an Isco 12 g silica cartridge eluting with 3:2 hexane/ethyl acetate to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748443B2
Source datasetuspto-grants-2014_06
ORD IDord-b056734448c74cf6b00761ba4572fe0a
Source noteuspto-grants-2014_06