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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 346668Erstellt: 26. Oktober 2026

Triphenylphosphine → tert-butyl N-{3-[1-(4-pyridyl)piperidin-4-yloxy]phenyl}carbamate

https://huagongshe.com/reaction/346668

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Eduktethyl N-ethoxycarbonyliminocarbamateHCID 220568—
Edukttert-butyl N-(3-hydroxyphenyl)carbamateHCID 312485—
Edukt1-(Pyridin-4-yl)piperidin-4-olHCID 23447619—
LösungsmittelTetrahydrofuranHCID 8028—
Produkttert-butyl N-{3-[1-(4-pyridyl)piperidin-4-yloxy]phenyl}carbamateHCID 1791578566,2%

Reaktionsbedingungen

Temperatur4 °C

Reaktionsschritte

Diethyl azodicarboxylate (3 ml) was added over 15 minutes to a stirred mixture of 1-(4-pyridyl)piperidin-4-ol (3.39 g), 3-(N-tert-butoxycarbonylamino)phenol (Chemical Abstracts, vol. 119, abstract 139113; PCT Patent Application WO 9306085; 3.98 g), triphenylphosphine (4.99 g) and THF (150 ml) which had been cooled to 4° C. The resultant mixture was stirred for 48 hours at ambient temperature. The solvent was evaporated and the residue was purified by column chromatography using a 9:1 mixture of methylene chloride and methanol as eluent. The resultant foam was crystallised from diethyl ether to give tert-butyl N-{3-[1-(4-pyridyl)piperidin-4-yloxy]phenyl}carbamate (4.65 g), m.p. 165-166° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07173025B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-824e5e37bf714049a6b5762aa95f07f4
Quellennotizuspto-grants-2007_02