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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1049611Erstellt: 26. Oktober 2026

Ammonium Chloride → 1-(2'-Fluoro-5'-methoxy-4-((4-methoxybenzyl)oxy)-[1,1'-biphenyl]-2-yl)-4,4-dimethylpentan-1-ol

https://huagongshe.com/reaction/1049611

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmonium ChlorideHCID 25517—
EduktHCID 117759914HCID 117759914—
EduktHCID 178444610HCID 178444610—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-(2'-Fluoro-5'-methoxy-4-((4-methoxybenzyl)oxy)-[1,1'-biphenyl]-2-yl)-4,4-dimethylpentan-1-olHCID 117759870—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

A solution of (3,3-dimethylbutyl)magnesium chloride in THF (0.50 M, 13.1 mL) was added to a solution of 2′-fluoro-5′-methoxy-4-((4-methoxybenzyl)oxy)-[1,1′-biphenyl]-2-carbaldehyde (800 mg) in THF (15 mL) at 0° C., and the mixture was stirred at 0° C. for 50 min. To the reaction mixture was added saturated aqueous ammonium chloride solution at 0° C., and the mixture was extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (788 mg) as a pale-yellow oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09382188B2
Quelldatensatzuspto-grants-2016_07
ORD IDord-8336a7f8b5604c4aa6fb7fe4bc580b19
Quellennotizuspto-grants-2016_07