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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611116Generated: November 3, 2026

Sodium Iodide → 1-[2,6-bis(benzyloxy)phenyl]ethanone

https://huagongshe.com/reaction/1611116

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantBenzyl BromideHCID 7498—
ReactantPotassium CarbonateHCID 11430—
Reactant2',6'-DihydroxyacetophenoneHCID 69687—
SolventAcetoneHCID 180—
Product1-[2,6-bis(benzyloxy)phenyl]ethanoneHCID 83886691.4%

Reaction Steps

A suspension of (2′,6′-dihydroxy)acetophenone (25.0 g, 164 mmol), benzyl bromide (40 mL, 337 mmol), potassium carbonate (136 g, 986 mmol) and sodium iodide (2.5 g, 16 mmol) in acetone (500 mL) was stirred at reflux overnight. The mixture was concentrated under reduced pressure, and diluted with ethyl acetate (500 mL) and water (250 mL). The separated aqueous phase was extracted with ethyl acetate (200 mL×2). The combined organic phase was washed with brine (100 mL), dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was triturated with hexane, collected by filtration, washed with hexane and dried under reduced pressure to give 1-[2,6-bis(benzyloxy)phenyl]ethanone (24.9 g, yield; 46%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984649B1
Source datasetuspto-grants-2006_01
ORD IDord-817a7e95534548a78452afe52a8b0d5c
Source noteuspto-grants-2006_01