HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 386534Generated: November 1, 2026
Sodium borohydride → Tert-butyl 4-hydroxy-2-methylpiperidine-1-carboxylate
https://huagongshe.com/reaction/386534
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | tert-Butyl 2-methyl-4-oxopiperidine-1-carboxylate | HCID 12992764 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 4-hydroxy-2-methylpiperidine-1-carboxylate | HCID 22181172 | 101.5% |
Reaction Steps
To a solution of tert-butyl 2-methyl-4-oxopiperidine-1-carboxylate (727 mg, 3.41 mmol, Small Molecules Inc.) in MeOH (6.0 mL) at 0° C. was added sodium borohydride (193 mg, 5.11 mmol, Aldrich) in several portions. The reaction mixture was stirred at 0° C. for 1 hr and warmed up to room temperature and continuously stirred for another 2.5 hrs. The resulting mixture was then quenched with saturated NH4Cl aqueous solution and evaporated under reduced pressure to remove MeOH followed by extraction with CH2Cl2 (3×). The combined extracts were dried (Na2SO4) and concentrated in vacuo to give the title compound (745 mg) as a colorless sticky oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372837B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-1b1d7a841b854dd2856015d2459a8921 |
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| Source note | uspto-grants-2013_02 |
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