Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2368080Generated: October 30, 2026

Sodium borohydride → tert-Butyl 4-(3-hydroxybutyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2368080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant1196894-98-0HCID 57517482—
SolventEthanolHCID 702—
Producttert-Butyl 4-(3-hydroxybutyl)piperidine-1-carboxylateHCID 5751748399.5%

Reaction Steps

To a solution of tert-butyl 4-(3-oxobutyl)piperidine-1-carboxylate (3.7 g) in ethanol (40 mL) was added sodium borohydride (550 mg) at room temperature, and the mixture was stirred at room temperature for 30 min. The solvent was evaporated under reduced pressure and the residue was dissolved in ethyl acetate and water. The organic layer was separated, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give the title compound (3.71 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08703758B2
Source datasetuspto-grants-2014_04
ORD IDord-46f736bc081045c9b01ac205f82d435e
Source noteuspto-grants-2014_04