HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515585Generated: October 30, 2026
Sodium borohydride → (2S,5S)-1-tert-butyl 2-ethyl 5-hydroxypiperidine-1,2-dicarboxylate
https://huagongshe.com/reaction/515585
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (S)-1-tert-butyl 2-ethyl 5-oxopiperidine-1,2-dicarboxylate | HCID 70701166 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (2S,5S)-1-tert-butyl 2-ethyl 5-hydroxypiperidine-1,2-dicarboxylate | HCID 86700663 | 81.5% |
Reaction Steps
NaBH4 (36 g, 1.0 mol) was added in portions to a solution of (S)-1-tert-butyl 2-ethyl 5-oxopiperidine-1,2-dicarboxylate (250 g, 0.92 mol) in EtOH (1500 mL) at −40° C. The reaction mixture was then stirred at −40° C. for 0.5 hr then quenched with 10% HOAc solution. After diluting with water, the mixture was extracted with DCM three times. The combined organic layer was concentrated in vacuum and purified by silica gel column chromatography (1:1 petroleum ether/EtOAc) to afford (2S,5S)-1-tert-butyl 2-ethyl 5-hydroxypiperidine-1,2-dicarboxylate (205 g, 80%) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09108966B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-d3570c7021b64bb9b01f448341cdfdb9 |
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| Source note | uspto-grants-2015_08 |
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