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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510873Generated: October 30, 2026

Ethylene Glycol → 1-[5-Chloro-3-(4-hydroxypiperidin-1-yl)-2-methoxy-4-methylphenyl]ethanone

https://huagongshe.com/reaction/510873

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantPiperidin-4-olHCID 79341—
Reactant1-(5-Chloro-3-iodo-2-methoxy-4-methylphenyl)ethanoneHCID 86666797—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
Product1-[5-Chloro-3-(4-hydroxypiperidin-1-yl)-2-methoxy-4-methylphenyl]ethanoneHCID 8666679811%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a mixture of 1-(5-chloro-3-iodo-2-methoxy-4-methylphenyl)ethanone (150 mg, 0.46 mmol) and 4-hydroxypiperidine (56 mg, 0.56 mmol) in isopropyl alcohol (1 mL) was added 1,2-ethanediol (0.052 mL, 0.92 mmol), potassium phosphate (200 mg, 0.93 mmol), and copper(I) iodide (5 mg, 0.02 mmol). The reaction was heated at 80° C. overnight and then cooled to room temperature. Water was added, and the mixture was extracted with ethyl acetate. The combined organic phases were washed with brine and dried over sodium sulfate, filtered and concentrated to dryness. The residue was purified on silica gel, eluting with 0 to 50% ethyl acetate in hexanes, to give the desired product (15 mg, 11%). LCMS calculated for C15H21ClNO3 (M+H)+: m/z=298.1. found: 298.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-26acb8478a754a1c84d29b4280ca02fb
Source noteuspto-grants-2015_08