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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179255Generated: October 30, 2026

1,10-Phenanthroline → 1-methoxy-4-[(2-methylprop-2-en-1-yl)oxy]benzene

https://huagongshe.com/reaction/2179255

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantMethallyl alcoholHCID 10557—
ReactantCesium carbonateHCID 10796—
Reactant4-IodoanisoleHCID 69676—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
Product1-methoxy-4-[(2-methylprop-2-en-1-yl)oxy]benzeneHCID 25796278%

Reaction Conditions

Temperature110 °C

Reaction Steps

A test tube was charged with CuI (20 mg, 0.10 mmol, 0.10 equiv), 1,10-phenanthroline (36 mg, 0.20 mmol, 0.20 equiv), Cs2CO3 (652 mg, 2.0 mmol, 2.0 equiv), 4-iodoanisole (234 mg, 1.0 mmol, 1.0 equiv), 2-methyl-2-propen-1-ol (168 μL, 2.0 mmol, 2.0 equiv) and toluene (0.5 mL). The test tube was sealed and the reaction mixture was stirred at 110° C. for 28 h. The resulting suspension was cooled to room temperature and filtered through a 0.5×1 cm pad of silica gel, eluting with diethyl ether. The filtrate was concentrated in vacuo. Purification of the residue by flash chromatography on silica gel (2×20 cm; pentane:diethyl ether 30:1) provided 139 mg (78% yield) of the title compound as a colorless solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067955B2
Source datasetuspto-grants-2015_06
ORD IDord-d9bc3bcd3e734523874116f6f2861512
Source noteuspto-grants-2015_06