Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1255086Erstellt: 26. Oktober 2026

Triphenylphosphine → (R)-((R)-quinuclidin-3-yl) 2-(4-fluorophenylamino)-2-phenylacetate

https://huagongshe.com/reaction/1255086

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
Edukt3-Quinuclidinol, (+)-HCID 736411—
EduktDiethyl azodicarboxylateHCID 5462977—
Edukt(R)-(4-fluoro-phenylamino)-phenyl-acetic acidHCID 7006576—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(R)-((R)-quinuclidin-3-yl) 2-(4-fluorophenylamino)-2-phenylacetateHCID 5940113379,2%

Reaktionsschritte

To a solution of (R)-(4-fluoro-phenylamino)-phenyl-acetic acid (I253) (420 mg, 1.71 mmol) in dry THF (40 mL), are sequentially added (S)-quinuclidin-3-ol (218 mg, 1.71 mmol), DEAD (407 ul, 2.57 mmol) and triphenylphosphine (674 mg, 2.57 mmol). The reaction is refluxed for 30 minutes under N2 flowstream and then the solvent is evaporated. The residue is partitioned between water and EtOAc, the organic layer is separated, dried over Na2SO4, filtered and evaporated to dryness. The resulting crude is purified by flash chromatography (DCM/MeOH=95/5) to obtain the title compound as a pale yellow oil (480 mg, 79% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08455646B2
Quelldatensatzuspto-grants-2013_06
ORD IDord-9bc76f026041427d85a93ef3e5255325
Quellennotizuspto-grants-2013_06