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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403827Generated: November 1, 2026

1-((Phenylmethoxy)carbonyl)-3-piperidinebutanoic acid → Phenylmethyl 3-(4-hydroxybutyl)-1-piperidinecarboxylate

https://huagongshe.com/reaction/2403827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-((Phenylmethoxy)carbonyl)-3-piperidinebutanoic acidHCID 44890831—
SolventTetrahydrofuranHCID 8028—
ProductPhenylmethyl 3-(4-hydroxybutyl)-1-piperidinecarboxylateHCID 58306139—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-(1-{[(phenylmethyl)oxy]carbonyl}-3-piperidinyl)butanoic acid (5.01 g, 16.41 mmol) in dry THF (40 ml) at 0° C. under nitrogen was added a solution of Borane-THF complex, (1M soln. in THF) (49.2 ml, 49.2 mmol), dropwise over 1 hour. The mixture was allowed to stir at 0° C. and gradually allowed to warm to rt over 20 hours. The mixture was cooled in an ice bath and cautiously quenched with dropwise addition of MeOH (20 ml) stirred in the cold bath for 2 hours then quenched further with 10% 2N HCl/MeOH (20 ml), stirred for 1 hour at rt and evaporated under reduced pressure. The residue was co-evaporated with methanol several times.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802684B2
Source datasetuspto-grants-2014_08
ORD IDord-a5b01dad871642769e7300f04eefed21
Source noteuspto-grants-2014_08