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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2366529Generated: October 27, 2026

Ethanolamine → Benzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylate

https://huagongshe.com/reaction/2366529

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantSodium HydroxideHCID 14798—
ReactantBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Solvent1,2-DichloroethaneHCID 11—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductBenzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylateHCID 22137568107.7%

Reaction Steps

A solution of benzyl 4-oxopiperidin-1-carboxylate (7.0 g), 2-aminoethanol (2.8 g) and acetic acid (2.7 g) in 1,2-dichloroethane (150 mL)-methanol (10 mL) was stirred at room temperature for 3 hours, sodium triacetoxyborohydride (12.7 g) was added thereto, and the mixture was stirred at room temperature for 15 hours. A 1N sodium hydroxide solution was added to the reaction mixture, pH of the aqueous layer was adjusted to about 12, and then the organic layer was separated. The organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to obtain the title compound (9.0 g, quantitative) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697865B2
Source datasetuspto-grants-2014_04
ORD IDord-5bd7b5d179e447d3b72bdd6a86e7ed6a
Source noteuspto-grants-2014_04