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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 632559Generated: October 29, 2026

Benzyl 4-oxopiperidine-1-carboxylate → HCID 86686412, compound

https://huagongshe.com/reaction/632559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl alaninate hydrochlorideHCID 11275390—
Solvent1,1-DichloroethaneHCID 6365—
ProductHCID 86686412HCID 8668641297.5%

Reaction Steps

To a solution of N-Cbz-4-piperidinone (3.497 g, 15.0 mmol) in dichloroethane (100 mL) was added L-alanine tert-butyl ester hydrochloride (2.731 g, 15.03 mmol) and sodium triacetoxyborohydride (6.47 g, 30.5 mmol). The mixture was stirred for 20 hours at room temperature, then quenched by the addition of saturated ammonium chloride (100 mL). The mixture was poured into ethyl acetate (500 mL), washed with water (2 times 100 mL), dried (MgSO4) and concentrated to yield the desired product (5.30 g, 97% yield). LC/MS: m/z 325.25 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09321718B2
Source datasetuspto-grants-2016_04
ORD IDord-38ae7e601b8e48c7a7adddb1370eddf7
Source noteuspto-grants-2016_04