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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1473783Generated: October 25, 2026

Sodium borohydride → 1-Methoxypiperidin-4-ol

https://huagongshe.com/reaction/1473783

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1-Methoxypiperidin-4-oneHCID 19936653—
SolventEthanolHCID 702—
Product1-Methoxypiperidin-4-olHCID 3022606—

Reaction Steps

To a solution of 1-methoxy-piperidin-4-one [prepared according to Journal of Organic Chemistry (1961), 26, 1867-74] (15.0 g, 116.1 mmol) in ethanol (430 ml) was added sodium borohydride 96% (2.29 g, 58.1 mmol) in portions. The reaction mixture was stirred at room temperature for 5 hours, evaporated to half of its volume, poured on cold saturated aqueous ammonium chloride and thoroughly extracted with ethyl acetate. The combined organic layers were washed with brine, dried over sodium sulfate and concentrated. The residue was purified by chromatography on silica gel (ethyl acetate). Yield: 10.9 g of 1-methoxy-piperidin-4-ol as a liquid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018135B2
Source datasetuspto-grants-2015_04
ORD IDord-68199146adf349e895f22e1e5de378d0
Source noteuspto-grants-2015_04