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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 20216Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/20216

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolamineHCID 700—
EduktSodium HydroxideHCID 14798—
EduktBenzyl 4-oxopiperidine-1-carboxylateHCID 643496—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelMethanolHCID 887—
ProduktBenzyl 4-[(2hydroxyethyl)amino]piperidin-1-carboxylateHCID 22137568107,7%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07745623B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-75db2ba6c6b64dc88b6623abe37c1296
Quellennotizuspto-grants-2010_06