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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 3-(3,4-Dichlorophenyl)-3-(2-(t-butyldimethylsilyloxy)ethyl)-6-oxopiperidine | HCID 18464740 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | Oxolane--water (1/1) | HCID 21881883 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-[3-(3,4-Dichlorophenyl)piperidin-3-yl]ethanol | HCID 15460400 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06211199B1 |
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| Source dataset | uspto-grants-2001_04 |
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| ORD ID | ord-6bffba62f0374b65b5423a79f7662d90 |
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| Source note | uspto-grants-2001_04 |
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