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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574173Generated: October 29, 2026

tert-Butyl 4-oxopiperidine-1-carboxylate → Tert-butyl 4-hydroxypiperidine-1-carboxylate

https://huagongshe.com/reaction/574173

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
ProductTert-butyl 4-hydroxypiperidine-1-carboxylateHCID 64350297.4%

Reaction Steps

To a solution of tert-butyl 4-oxopiperidine-1-carboxylate (10 g, 50 mmol) in CH3OH (100 mL) was added NaBH4 (5.7 g, 150 mmol) portionwise carefully and the mixture was stirred at rt for 3 h. The reaction was quenched by carefully pouring into ice-water (100 mL) and organic solvent was removed under reduced pressure. The aqueous phase was neutralized to pH=7 with 1N HCl and extracted with DCM/MeOH (5×60 mL, v/v=10/1). The combined organic layers were washed with brine (30 mL), dried over anhydrous Na2SO4, filtered and concentrated under reduced pressure to afford the crude product (9.8 g, 97%) as a white solid. [LCMS: Rt=1.36 min, m/z 146.1 (M-Bu+H)]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09034874B2
Source datasetuspto-grants-2015_05
ORD IDord-345412a625c54bd183ed9f6c7e919856
Source noteuspto-grants-2015_05