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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 660703Erstellt: 27. Oktober 2026

Butyrophenone → 2-(3-Benzyloxy-4-nitrobenzyl)-1-phenylbutan-1-one

https://huagongshe.com/reaction/660703

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyrophenoneHCID 10315—
EduktLithium HexamethyldisilazideHCID 2733832—
Edukt2-Benzyloxy-4-bromomethyl-1-nitrobenzeneHCID 62115042—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-(3-Benzyloxy-4-nitrobenzyl)-1-phenylbutan-1-oneHCID 68837950—

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

To a solution of 1-phenylbutan-1-one (203 mg, 1.37 mmol) in THF (2.5 mL) at −78° C. is added dropwise LiHMDS (1.62 mL of 1.0 M solution in THF, 1.62 mmol) over a period of 15 min. The solution is stirred at −78° C. for 1 h then a solution of 2-benzyloxy-4-bromomethyl-1-nitrobenzene (Example 83, step C) (400 mg, 1.25 mmol) in THF (2.5 mL) is added dropwise. The mixture is allowed to warm to RT and stirred there for 1 h then is quenched with saturated ammonium chloride solution. The mixture is extracted with EtOAc and the organic phase is washed with brine then dried over magnesium sulfate. The solvent is removed under reduced pressure and the residue is purified by flash chromatography using a gradient of 5-100% EtOAc/hexane as eluent to give the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08084448B2
Quelldatensatzuspto-grants-2011_12
ORD IDord-8d07e62cd094468fb85af82de7512bca
Quellennotizuspto-grants-2011_12