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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 602182Erstellt: 24. Oktober 2026

Triphenylphosphine → HCID 58992609, Verbindung

https://huagongshe.com/de/reaction/602182

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt4'-Chloro-4-biphenylolHCID 91589—
Edukttert-Butyl 3-(hydroxymethyl)piperidine-1-carboxylateHCID 2763851—
Eduktethyl (NE)-N-ethoxycarbonyliminocarbamate;tolueneHCID 87147022—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 58992609HCID 5899260967%

Reaktionsschritte

1-(tert-Butoxycarbonyl)piperidin-3-ylmethanol (323 mg, 1.50 mmol) and 4′-chloro-4-hydroxybiphenyl (307 mg, 1.50 mmol) were suspended in tetrahydrofuran (15 mL). To this suspension, triphenylphosphine (608 mg, 2.25 mmol) was added and the mixture was stirred at room temperature for 10 min. A 40% diethylazodicarboxylate/toluene solution (1.36 mL, 3.00 mmol) was then added and the mixture was stirred at room temperature for 16 hours. Subsequently, water was added and the mixture was extracted with ethyl acetate. The extract washed with brine, followed by drying over magnesium sulfate and evaporation of the solvent. Purification of the resulting residue by silica gel column chromatography (hexane:ethyl acetate=50:1->10:1) gave 401 mg (67%) of the desired compound as a colorless powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07902367B2
Quelldatensatzuspto-grants-2011_03
ORD IDord-d32fc68c954446ddb5732ec013f856ee
Quellennotizuspto-grants-2011_03