Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496624Generated: October 30, 2026

1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acid → Tert-butyl 4-(hydroxymethyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/496624

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(tert-Butoxycarbonyl)-4-piperidinecarboxylic acidHCID 392871—
ReactantBorane;tetrahydrofuranHCID 2723981—
SolventTetrahydrofuranHCID 8028—
ProductTert-butyl 4-(hydroxymethyl)piperidine-1-carboxylateHCID 276408185%

Reaction Conditions

Temperature0 °C

Reaction Steps

1-Boc-isonipecotic acid (10.0 g, 214 mmol) was dissolved in THF (400 mL) and cooled to 0° C. A solution of BH3-THF (180 mL, 1 N in THF, 180 mmol) was added slowly. The mixture stirred for 1 h at 0° C. and was allowed to warm to room temperature for 12 h. The mixture was carefully quenched with water and diluted with ethyl acetate. The water layer was extracted with ethyl acetate. The organic layers were combined, washed with brine, dried (Na2SO4), filtered and concentrated to provide 1-Boc-piperidine-4-methanol (7.98 g, 85%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946467B2
Source datasetuspto-grants-2005_09
ORD IDord-02eb9337cb784655b0583322eb00867d
Source noteuspto-grants-2005_09