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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1477594Generated: October 30, 2026

2-(Dimethylamino)ethanol → 1-(4-Fluorophenyl)pyrrolidin-3-ol

https://huagongshe.com/reaction/1477594

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
Reactant4-FluoroiodobenzeneHCID 9605—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant4-HydroxypyrrolidineHCID 98210—
CatalystCopperHCID 23978—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Fluorophenyl)pyrrolidin-3-olHCID 66961704—

Reaction Conditions

Temperature110 °C

Reaction Steps

Under nitrogen atmosphere, a 1,4-dioxane suspension of 1-fluoro-4-iodobenzene (2.00 g, 9.01 mmol), pyrrolidin-3-ol (785 mg, 9.01 mmol), potassium phosphate (3.83 g, 18.0 mmol), copper (I) iodide (343 mg, 1.80 mmol), copper (114 mg, 1.80 mmol), and N,N-dimethylaminoethanol (100 mg) was stirred at 90° C. for 1 day and at 110° C. for 5 hours. After completion of the reaction, the reaction solution was filtered with Celite and the filtrate was concentrated under reduced pressure. To the residue, water was added and extraction with ethyl acetate from the resultant mixture was performed. The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to obtain a crude product of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09403798B2
Source datasetuspto-grants-2016_08
ORD IDord-bf42c3591c1b4c13bac01b5524e9e76d
Source noteuspto-grants-2016_08