Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405696Generated: October 26, 2026

Cuminol → 3-{[4-(1-Methylethyl)benzyl]oxy}pyridin-2-amine

https://huagongshe.com/reaction/1405696

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCuminolHCID 325—
Reactant1,10-PhenanthrolineHCID 1318—
ReactantCesium carbonateHCID 10796—
Reactant2-Amino-3-bromopyridineHCID 817700—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
SolventSodium chloride; waterHCID 57417360—
Product3-{[4-(1-Methylethyl)benzyl]oxy}pyridin-2-amineHCID 2898179265.7%

Reaction Conditions

Temperature110 °C

Reaction Steps

A mixture of cesium carbonate (2.82 g), 1,10-phenanthrolin (0.208 g), (4-isopropylphenyl)methanol (8.68 g), 3-bromopyridin-2-amine (1 g) and copper (I) iodide (0.110 g) in toluene (10 mL) was stirred under a nitrogen atmosphere at 110° C. overnight, and at 130° C. for 5 hr. The reaction mixture was added to saturated brine, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (0.92 g) as a pale-yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916551B2
Source datasetuspto-grants-2014_12
ORD IDord-cf3476a2b0734bb5a6812b2c7b8db6de
Source noteuspto-grants-2014_12