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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 419313Erstellt: 23. Oktober 2026

Triphenylphosphine → HCID 59452627, Verbindung

https://huagongshe.com/de/reaction/419313

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt3-Methyl-4-nitrophenolHCID 17412—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
EduktBenzyl 4-Hydroxy-1-piperidinecarboxylateHCID 2794620—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 59452627HCID 5945262787%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

3-Methyl-4-nitrophenol (1.74 g, 11.4 mmol), triphenylphosphine (5.98 g, 22.8 mmol), and phenylmethyl 4-hydroxy-1-piperidinecarboxylate (3.99 g, 17.0 mmol) were dissolved in DCM with stirring and cooled to 0° C. Diisopropyl azodicarboxylate (3.35 mL, 17.0 mmol) was added via syringe. The reaction was stirred for 10 min and allowed to warm to rt. The reaction was stirred overnight and adsorbed onto silica gel. The crude material was purified by flash chromatography, and fractions containing product were concentrated in vacuo. The material was contaminated with 3-methyl-4-nitrophenol. The material was dissolved in diethyl ether and washed with 2N NaOH solution (3×), H2O, and brine. The organic layer was dried over MgSO4, filtered, and concentrated in vacuo to provide 3.67 g (87%) of the title compound. 1H NMR (400 MHz, DMSO-d6) δ 8.02 (d, J=9.0 Hz, 1H), 7.42-7.24 (m, 5H), 7.06 (d, J=2.4 Hz, 1H), 7.01 (dd, J=9.1, 2.7 Hz, 1H), 5.07 (s, 2H), 4.76 (ddd, J=7.7, 4.2, 4.0 Hz, 1H), 3.81-3.64 (m, 2H), 3.31 (br. s., 2H), 2.52 (s, 3H), 2.01-1.88 (m, 2H), 1.63-1.49 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093239B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-d6bad6fa66c74a7881dd631728f4e66b
Quellennotizuspto-grants-2012_01