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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 521937Erstellt: 24. Oktober 2026

Triphenylphosphine → HCID 86713875, Verbindung

https://huagongshe.com/de/reaction/521937

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriphenylphosphineHCID 11776—
EduktDiisopropyl diazene-1,2-dicarboxylateHCID 75555—
Edukt(-)-3-HydroxytetrahydrofuranHCID 641512—
EduktMethyl 2-(2,6-difluoro-4-hydroxyphenyl)thiazole-4-carboxylateHCID 136377230—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 86713875HCID 86713875—

Reaktionsschritte

To a solution of methyl 2-(2,6-difluoro-4-hydroxy-phenyl)thiazole-4-carboxylate (207 mg, 0.763 mmol) and (R)-3-hydroxytetrahydrofuran (3 equiv., 206 mg) in tetrahydrofuran (5 mL) was added triphenylphosphine (3 equiv., 600 mg) and diisopropyl azodicarboxylate (3 equiv., 0.45 mL) The mixture was stirred at RT for 2 days. The mixture was concentrated and partitioned between EtOAc and water. The organic layer was washed with sat. NaHCO3, brine, dried over Na2SO4 and concentrated. This residue was diluted with THF (3 mL) and water (1 mL) and LiOH (36 mg) was added. After stirring at rt for 2.5 hours, the reaction was neutralized with 1 N HCl(aq), diluted with EtOAc and washed with brine. The organic extracts were dried (Na2SO4) and concentrated in vacuo to provide the title compound, contaminated with triphenylphosphine oxide, and other by-products, which was used without further purification.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328106B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-ebe1ff9fcb5a4c20b9cbe9433f928802
Quellennotizuspto-grants-2016_05