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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39024Generated: October 25, 2026

Water → 1-[5-Bromo-3-chloro-2-(oxiran-2-ylmethoxy)phenyl]ethanone

https://huagongshe.com/reaction/39024

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantGlycidyl tosylate, (R)-HCID 154187—
Reactant1-(5-Bromo-3-chloro-2-hydroxyphenyl)ethan-1-oneHCID 24211939—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-[5-Bromo-3-chloro-2-(oxiran-2-ylmethoxy)phenyl]ethanoneHCID 8665295274.7%

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-(5-bromo-3-chloro-2-hydroxyphenyl)ethanone (5.5 g, 21.9 mmol), (2R)-(−)Glycidyltosylate (10 g, 43.8 mmol) and K2CO3 (4.5 g, 32.9 mmol) in DMF (25 ml) was heated at 60° C. for 25 h. The solution was brought to ambient temperature and water and EtOAc was added. The water phase was extracted with EtOAc. The combined organic phases were washed with LiCl (5%), HCl (1 N) and brine and then dried (Na2SO4) and evaporated to dryness. Purification on flash column chromatography (isooctane/EtOAc) gave the title compound (5.0 g). MS m/z (rel. intensity, 70 eV) 250 (30), 248 (M+, 26), 235 (bp), 233 (85), 57 (90), 306 (M+, 9).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524766B2
Source datasetuspto-grants-2013_09
ORD IDord-1b945c0045fd4c1786013a469ac47a59
Source noteuspto-grants-2013_09