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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 323253Generated: October 31, 2026

Sulfuric Acid → 2-[3-(3,4-Dichlorophenyl)piperidin-3-yl]ethanol

https://huagongshe.com/reaction/323253

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
Reactant3-(3,4-Dichlorophenyl)-3-(2-(t-butyldimethylsilyloxy)ethyl)-6-oxopiperidineHCID 18464740—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantOxolane--water (1/1)HCID 21881883—
SolventTetrahydrofuranHCID 8028—
Product2-[3-(3,4-Dichlorophenyl)piperidin-3-yl]ethanolHCID 15460400—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Combine a solution of lithium aluminum hydride (42 mL, 1 M in THF, 42.0 mmol). Cool to about −10° C. using an isopropyl alcohol/ice bath. Slowly add a solution of sulfuric acid (1.15 mL, 21.6 mmol) in tetrahydrofuran (4 mL) at such a rate that the reaction temperature does not rise above −10° C. Stir vigorously and warm to ambient temperature. After 2 hours, add a solution of 3-(3,4-dichlorophenyl)-3-(2-(t-butyldimethylsilyloxy)ethyl)-6-oxopiperidine (5.56 g, 13.85 mmol) in tetrahydrofuran (12 mL). Heat to reflux. After 18 hours, add 1/1 tetrahydrofuran/water. After 1 hour, filter and rinse with dichloromethane. Suspend the solids removed by filtration in tetrahydrofuran (400 mL). To the tetrahydrofuran suspension add water (20 mL) and 15% aqueous sodium hydroxide solution (8 mL) and stir vigorously. After 2 hours, filter. Combine the filtrates and concentrate in vacuo to give an aqueous suspension. Extract twice with dichloromethane. Dry the organic layers over Na2SO4, filter, and concentrate in vacuo to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06211199B1
Source datasetuspto-grants-2001_04
ORD IDord-6bffba62f0374b65b5423a79f7662d90
Source noteuspto-grants-2001_04