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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 965791Erstellt: 25. Oktober 2026

Triethylamine → Benzyl [1-(3,3-dimethyl-2-oxobutyl)piperidin-4-yl]methylcarbamate

https://huagongshe.com/reaction/965791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBromopinacoloneHCID 21642—
EduktBenzyl (piperidin-4-ylmethyl)carbamateHCID 14809798—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzyl [1-(3,3-dimethyl-2-oxobutyl)piperidin-4-yl]methylcarbamateHCID 86759854100%

Reaktionsschritte

To a solution of benzyl piperidin-4-ylmethylcarbamate (Tetrahedron Lett. 1990, 31, 6903, 6.9 g, 27.8 mmol) in N,N-dimethylformamide (60 mL) were added triethylamine (9.7 mL, 69.5 mmol) and 1-bromo-3,3-dimethylbutan-2-one (7.9 g, 41.7 mmol) at room temperature. The mixture was stirred at room temperature for 2 h and quenched with water (60 mL) followed by extraction with ethyl acetate-toluene mixture (3×30 mL). Concentration and purification by column chromatography on silica gel eluting with ethyl acetate/hexane (2:1) gave the title compound (9.6 g, 100%) as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06951867B2
Quelldatensatzuspto-grants-2005_10
ORD IDord-59257743e704426aa36095b637a36c73
Quellennotizuspto-grants-2005_10