HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 225810Generated: October 30, 2026
Tert-butyl 4-hydroxypiperidine-1-carboxylate → Ammonia
https://huagongshe.com/reaction/225810
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-butyl 4-hydroxypiperidine-1-carboxylate | HCID 643502 | — |
| Reactant | 4-Chloro-2,3-dimethylpyridine | HCID 22660262 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ammonia | HCID 222 | — |
| Product | HCID 57753825 | HCID 57753825 | — |
Reaction Steps
Potassium tert-butoxide (4.70 g, 42 mmol) was added to a solution of 1-Boc-4-hydroxypiperidine (4.05 g, 20.1 mmol) in dimethylsulfoxide (20 mL) and the mixture was stirred at room temperature for 1 hour. 4-Chloro-2,3-dimethylpyridine (3.58 g, 20.1 mmol) was then added and the reaction mixture was stirred at 50° C. for 18 hours. The mixture was partitioned between ethyl acetate and water, and the organic layer was separated and washed with sodium hydrogen carbonate solution and brine. The organic solution was then dried over magnesium sulfate concentrated in vacuo and the residue was purified by column chromatography on silica gel, eluting with dichloromethane:methanol:0.88 ammonia, 100:0:0 to 94:6:0.6, to afford the title compound as an oil in 39% yield, 2.4 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07557131B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-23a0472d11f4437ba71369ba854a3108 |
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| Source note | uspto-grants-2009_07 |
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