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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842314Generated: November 4, 2026

2-Methoxyethylamine → tert-Butyl 4-[(2-methoxyethyl)amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1842314

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyethylamineHCID 8018—
Reactanttert-Butyl 4-oxopiperidine-1-carboxylateHCID 735900—
ReactantSodium borohydrideHCID 4311764—
SolventMethanolHCID 887—
Producttert-Butyl 4-[(2-methoxyethyl)amino]piperidine-1-carboxylateHCID 43652134—

Reaction Steps

Amine preparation: 1-BOC-4-piperidinone (2.00 g) and 2-methoxyethylamine (872 μL) were stirred together in MeOH (20 mL) at room temperature overnight. Sodium borohydride (760 mg) was then added portionwise and the reaction mixture was allowed to stir further at ambient temperature. After 16 h, the solvent was removed in vacuo, the residue was diluted with DCM, washed with brine, dried (MgSO4) and the solvent removed in vacuo. The residue was purified using flash chromatography to yield 4-(2-methoxy-ethylamino)-piperidine-1-carboxylic acid tert-butyl ester as a colourless oil (1.69 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946217B2
Source datasetuspto-grants-2015_02
ORD IDord-04956b8faeb94b988df7db2aeb7c3eb4
Source noteuspto-grants-2015_02