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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 993193Erstellt: 24. Oktober 2026

tert-Butanol → Benzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylate

https://huagongshe.com/de/reaction/993193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktBenzyl 4-isocyanatopiperidine-1-carboxylateHCID 2776273—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzyl 4-((tert-butoxycarbonyl)amino)piperidine-1-carboxylateHCID 21981786—

Reaktionsschritte

A solution of 3.2 g (12.3 mmol) of (1-benzyloxycarbonylpiperidin-4-yl)isocyanate from Step A in 25 mL of DMF was slowly added to a suspension of CuCl3 in 25 mL of DMF and 12 mL of t-butanol. The reaction was stirred for 24 h and then diluted with water and extracted twice with 1:1 ether: ethyl acetate. The organic layers were each washed with a portion of water and brine, dried over sodium sulfate, combined and concentrated. The residue was purified by FC eluting with 20% ethyl acetate in hexanes to afford 685 mg of title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06472410B1
Quelldatensatzuspto-grants-2002_10
ORD IDord-c69a86db3f494bc6af5f4ea6a6877d96
Quellennotizuspto-grants-2002_10