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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2172117Erstellt: 25. Oktober 2026

Water → 1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-ol

https://huagongshe.com/reaction/2172117

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt3-Bromo-1-benzofuranHCID 640589—
Edukt1-(Diphenylmethyl)azetidin-3-oneHCID 3735558—
EduktButyllithiumHCID 178418339—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Benzhydryl-3-(benzofuran-2-yl)azetidin-3-olHCID 67154652—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

A 2.5 M solution of n-butyllithium in hexanes (2.23 mL, 5.58 mmol) was added dropwise to a solution of 3-bromobenzofuran (1.0 g, 5.08 mmol) in THF (35 mL) at −78° C. The reaction mixture was stirred for 30 minutes at −78° C. and then a solution of 1-benzhydrylazetidin-3-one (1.2 g, 5.08 mmol, as prepared in step 1 of example FAB270) in THF (10 mL) was added dropwise at the same temperature. The mixture was allowed to warm back to room temperature overnight. Water (50 mL) was added and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The residue was purified by chromatography on silica gel using petroleum ether/dichloromethane (50:50 to 0:100) as eluent. The title compound was obtained as a yellow solid (230 mg, 13%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09051321B2
Quelldatensatzuspto-grants-2015_06
ORD IDord-d66f2c0d0a9f4f6cb06764c9ea80419e
Quellennotizuspto-grants-2015_06