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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172288Generated: November 2, 2026

Acetic Acid → tert-Butyl 4-{[2-(2-nitrophenyl)ethyl]amino}piperidine-1-carboxylate

https://huagongshe.com/reaction/1172288

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant2-NitrophenethylamineHCID 12498123—
SolventMethanolHCID 887—
Producttert-Butyl 4-{[2-(2-nitrophenyl)ethyl]amino}piperidine-1-carboxylateHCID 18444265—

Reaction Steps

A stirred solution of 2-(2-nitrophenyl)ethanamine (4 g, 24 mmol) and tert-butyl 4-oxopiperidine-1-carboxylate (4.8 g, 24 mmol) in MeOH (48 ml) was brought to pH 5 by the addition of acetic acid. NaBH3CN (2.3 g, 36 mmol) was added and the reaction mixture was stirred at RT for 3 hours. The solvent was evaporated and the residue was taken up in EtOAc and sat. aq. Na2CO3. The layers were separated and the organic layer was washed with brine, dried (Na2SO4) and evaporated to dryness. Purification by column chromatography (0% to 7% MeOH in DCM) gave the desired product. LC/MS (10% to 99%): M/Z (M+H)+ (obs)=350; tR=2.22.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834000B2
Source datasetuspto-grants-2010_11
ORD IDord-0877491e71a14f6fb2b13f0e3cdb3fbe
Source noteuspto-grants-2010_11