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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095425Generated: October 31, 2026

Sodium Iodide → HCID 57861967, compound

https://huagongshe.com/reaction/1095425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
Reactant2-BromoethanolHCID 10898—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178516421HCID 178516421—
SolventDimethylformamideHCID 6228—
ProductHCID 57861967HCID 57861967—

Reaction Conditions

Temperature60 °C

Reaction Steps

A mixture of 1-(3,4-dichlorophenyl)-1H-pyrazol-3-ol (238 mg, 1.04 mmol; compound prepared in the same way as Example 1, Scheme 1-step 1B), 2-bromoethanol (273 mg, 2.08 mmol), potassium carbonate (0.43 g, 3.12 mmol) and sodium iodide (0.16 g, 1.04 mmol) in dimethylformamide (5 ml) was warmed, under dry nitrogen atmosphere, with stirring, to 60° C. overnight. The solvent was evaporated to dryness in vacuo and residue partitioned between water and ethyl ether. The combined organic phases were washed with water and dried over sodium sulphate, filtered and evaporated in vacuo. The residue was stirred with petroleum ether at 45° C. and decanted for 3 times to yield, after drying, 258 mg of 2-(1-(3,4-dichlorophenyl)-1H-pyrazol-3-yloxy)ethanol which was used without further purification in the next step of synthesis

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138186B2
Source datasetuspto-grants-2012_03
ORD IDord-35a8c0e28261433694f8d9ecea587767
Source noteuspto-grants-2012_03