Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1682677Erstellt: 26. Oktober 2026

Triethylamine → t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate

https://huagongshe.com/reaction/1682677

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktBenzyl chloroformateHCID 10387—
EduktSodium BicarbonateHCID 516892—
EduktTert-butyl (piperidin-4-yloxy)-acetateHCID 10036224—
LösungsmittelDichloromethaneHCID 6344—
Produktt-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetateHCID 10066408495,6%

Reaktionsschritte

t-Butyl 4-piperidinyloxyacetate (521 mg, 2.42 mmol) and triethylamine (0.40 ml, 2.9 mmol) were dissolved in methylene chloride (20 ml) and benzyloxycarbonyl chloride (0.41 mmol, 2.9 mmol) was added. The mixture was stirred at room temperature for 74 hours. A saturated aqueous sodium hydrogencarbonate solution (50 ml) was added to the reaction mixture and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine and dried over anhydrous magnesium sulfate. After filtration, low boiling matters were distilled away from the filtrate under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=2/1) to give 710 mg of t-butyl [N-benzyloxycarbonyl-4-piperidinyloxy]acetate as a colorless oil (84%). Methylene chloride (30 ml) and trifluoroacetic acid (10 ml) were added to this oil (692 mg, 1.99 mmol) and the mixture was stirred at room temperature for 17 hours. Low boiling matters were distilled away from the reaction mixture under reduced pressure to give 555 mg of [N-benzyloxycarbonyl-4-piperidinyloxy]acetate as a colorless solid (96%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05635527
Quelldatensatzuspto-grants-1997_06
ORD IDord-f771952f11b44a4b95182564668d31c2
Quellennotizuspto-grants-1997_06