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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactanttert-Butyl 2-methyl-4-oxopiperidine-1-carboxylateHCID 12992764—
SolventMethanolHCID 887—
ProductTert-butyl 4-hydroxy-2-methylpiperidine-1-carboxylateHCID 22181172101.5%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08372837B2
Source datasetuspto-grants-2013_02
ORD IDord-1b1d7a841b854dd2856015d2459a8921
Source noteuspto-grants-2013_02