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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670762Generated: November 1, 2026

Water → 4-(2H-1,3-Benzodioxol-5-yl)piperidin-4-ol

https://huagongshe.com/reaction/1670762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl 4-oxo-1-piperidinecarboxylateHCID 34767—
Reactant1-Bromo-3,4-(methylenedioxy)benzeneHCID 75831—
ReactantHCID 178418244HCID 178418244—
SolventTetrahydrofuranHCID 8028—
Product4-(2H-1,3-Benzodioxol-5-yl)piperidin-4-olHCID 1503471545.5%

Reaction Conditions

Temperature-78 °C

Reaction Steps

4-Bromo-1,2-(methylenedioxy)benzene (Tokyo Chemical Industry CO., LTD., 2.0 g) was dissolved in tetrahydrofuran (15 ml) and the mixture was cooled to −78° C. An n-butyllithium hexane solution (2.44 M, 5.7 ml) was added to the solution. The mixture was stirred at −78° C. for 1 hr, and 1-(ethoxycarbonyl)-4-piperidone (Aldrich Co., 1.7 g) was added. Then, the reaction temperature was raised to 0° C., and the mixture was further stirred for 1 hr. After completion of the reaction, water was added and the mixture was extracted three times with ethyl acetate. The organic layer was dried and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (elution solvent: hexane-ethyl acetate (5:1-2:1)). Then, the residue was dissolved in ethylene glycol (20 ml), a 50% aqueous potassium hydroxide solution was added, and the mixture was stirred with heating at 120° C. for 6 hr. After completion of the reaction, the mixture was extracted three times with chloroform. The organic layer was dried and the solvent was evaporated under reduced pressure to give 4-(1,3-benzodioxol-5-yl)piperidin-4-ol (1.0 g, yield 43%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994196B2
Source datasetuspto-grants-2011_08
ORD IDord-f5fc5cbec53844e7b034826221f9ae0b
Source noteuspto-grants-2011_08