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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1289807Generated: October 31, 2026

Potassium Iodide → [1-(4-Methyl-3-pentenyl)piperidin-4-yl] 2-cyclobutyl-2-hydroxy-2-phenylacetate

https://huagongshe.com/reaction/1289807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-methyl-2-penteneHCID 137521—
Reactant(Piperidin-4-yl) 2-cyclobutyl-2-hydroxy-2-phenylacetate hydrochlorideHCID 69831797—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product[1-(4-Methyl-3-pentenyl)piperidin-4-yl] 2-cyclobutyl-2-hydroxy-2-phenylacetateHCID 1892214361.4%

Reaction Conditions

Temperature70 °C

Reaction Steps

50 mg of (piperidin-4-yl) 2-cyclobutyl-2-hydroxy-2-phenylacetate hydrochloride, 25 mg of 5-bromo-2-methyl-2-pentene, 25 mg of potassium iodide and 47 mg of anhydrous potassium carbonate were suspended in 5 ml of anhydrous N,N-dimethylformamide, and this suspension was stirred at 70° C. for 3 hours. The reaction mixture was cooled to room temperature, mixed with water, and then extracted with diethyl ether. The organic layer was washed with a saturated aqueous solution of sodium chloride and then dried over anhydrous magnesium sulfate. After the solvent was distilled off under reduced pressure, the resulting residue was purified by silica gel column chromatography (developing solvent: chloroform/methanol=20/1) to obtain 35 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05750540
Source datasetuspto-grants-1998_05
ORD IDord-5a69668bbdd94a21845f8b021fa41096
Source noteuspto-grants-1998_05