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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 439412Erstellt: 25. Oktober 2026

Triphenylphosphine → N,O-bisphenyloxycarbonyl-t-butyloxycarbonylamino-2-propylhydroxylamine

https://huagongshe.com/reaction/439412

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiethyl azodicarboxylateHCID 5462977—
Edukttert-butyl N-(2-hydroxypropyl)carbamateHCID 9920508—
EduktN,O-Bis-(phenoxycarbonyl)-hydroxylamineHCID 10107329—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktN,O-bisphenyloxycarbonyl-t-butyloxycarbonylamino-2-propylhydroxylamineHCID 86749470836,9%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A one liter roundbottom flask was charged with N-Boc-1-amino-2-propanol (26.42 g, 0.0151 mol), triphenylphosphine (41.4 g, 0.158 mol), and N,O-bisphenyloxycarbonylhydroxylamine (43.2 g, 0.158 mol), and dry THF (550 mL). The solution was cooled to 0° C., and diethylazodicarboxylate (24.9 mL, 0.158 mol) was added in THF (50 mL). The reaction was stirred one hour after removing the cooling bath, and concentrated under vacuum. Chromatographic purification is enhanced by adding dichloromethane (200 mL) and concentrating in vacuo twice to remove THF before column chromatography (400 g silica gel, 15% EtOAc/Hex) to provide N,O-bisphenyloxycarbonyl-t-butyloxycarbonylamino-2-propylhydroxylamine (54.4 g, 80%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05514702
Quelldatensatzuspto-grants-1996_05
ORD IDord-fc2cceba9ecc4dca8fefd09f509b12a8
Quellennotizuspto-grants-1996_05