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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2179233Generated: October 27, 2026

Cesium carbonate → (R)-3-(1-phenylethoxy)anisole

https://huagongshe.com/reaction/2179233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantBenzene, 1-iodo-3-methoxy-HCID 69839—
Reactant5-Methyl-1,10-phenanthrolineHCID 72791—
Reactant1-Phenylethanol, (R)-HCID 637516—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventTolueneHCID 1140—
Product(R)-3-(1-phenylethoxy)anisoleHCID 1131073676%

Reaction Conditions

Temperature110 °C

Reaction Steps

A test tube was charged with CuI (20 mg, 0.10 mmol, 10 mol %), 5-methyl-1,10-phenanthroline (39 mg, 0.20 mmol, 20 mol %), Cs2CO3 (652 mg, 2.0 mmol), 3-iodoanisole (119 μL, 1.0 mmol), (R)-(+)-1-phenylethanol (205 μL, 1.7 mmol, >99% ee) and toluene (1 mL). The test tube was sealed and the reaction mixture was stirred at 110° C. for 32 h. The resulting suspension was cooled to room temperature and filtered through a 0.5×1 cm pad of silica gel eluting with ethyl acetate. The filtrate was concentrated. Purification of the residue by flash chromatography on silica gel (2×20 cm; hexane/ethyl acetate 30:1) provided 173 mg (76% yield, 98% ee) of the title compound as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09067955B2
Source datasetuspto-grants-2015_06
ORD IDord-c2b1277439004b45b1c2e47341bf1371
Source noteuspto-grants-2015_06