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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2376936Generated: October 30, 2026

Ethylene Glycol → HCID 21099458, compound

https://huagongshe.com/reaction/2376936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylene GlycolHCID 174—
ReactantPotassium CarbonateHCID 11430—
Reactant2-FluorothiophenolHCID 520216—
Reactant2-Chloro-5-iodopyridineHCID 4397176—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
SolventIsopropanolHCID 3776—
ProductHCID 21099458HCID 2109945867%

Reaction Steps

2-chloro-5-iodopyridine (3.0 g, 12.5 mmol), 2-fluorobenzenethiol (1.6 g, 12.5 mmol), potassium carbonate (3.45 g, 25.0 mmol), ethylene glycol (1.55 g, 25.0 mmol) and copper(I) iodide (0.12 g, 0.63 mmol) were stirred in refluxing isopropyl alcohol (50 mL) for 40 hours. Room temperature was attained, water was added and the products extracted into ethyl acetate (×2). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo while loading onto silica. Dry flash column chromatography using isohexane-2% ethyl acetate/isohexane gave 2-chloro-5-[(2-fluorophenyl)thio]pyridine as a pale yellow oil (2.0 g, 67%). δH (500 MHz, d6 DMSO): 7.25-7.29 (1H, m), 7.34-7.39 (1H, m), 7.44-7.51 (2H, m), 7.53 (1H, d, J=8.4 Hz), 7.75 (1H, dd, J=2.6, 8.4 Hz), 8.36 (1H, d, J=2.6 Hz); m/z (ES+) 240, 242 [MH+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07468393B2
Source datasetuspto-grants-2008_12
ORD IDord-05c5f7f725414f67bb913f8ba8dacd42
Source noteuspto-grants-2008_12