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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227896Erstellt: 25. Oktober 2026

Hydrogen Peroxide → (R)-1-(2',4'-Dichloro-biphenyl-4-yl)-hexane-1,6-diol

https://huagongshe.com/reaction/227896

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen PeroxideHCID 784—
EduktBoron trifluoride etherateHCID 8000—
EduktPotassium CarbonateHCID 11430—
EduktSodium HydroxideHCID 14798—
Edukt(R)-1-(2',4'-dichloro-biphenyl-4-yl)-hex-5-en-1-olHCID 57757255—
LösungsmittelWaterHCID 962—
LösungsmittelDiglymeHCID 8150—
LösungsmittelSodium borohydrideHCID 4311764—
Produkt(R)-1-(2',4'-Dichloro-biphenyl-4-yl)-hexane-1,6-diolHCID 25061620—

Reaktionsschritte

Impure (R)-1-(2′,4′-dichloro-biphenyl-4-yl)-hex-5-en-1-ol (1 g) was dissolved in 0.5 M NaBH4 in diglyme (9 mL) and chilled in an ice bath. BF3.OEt2 (1 mL) in diglyme (4 mL) was added with vigorous stirring. Stirring was continued for 1 hour and water (1 mL) was added. 3 M NaOH (2 mL) was added followed by 30% H2O2 (3 mL). Anhydrous K2CO3 (5 g) was added and the solvent was decanted. The K2CO3 was washed with ethyl acetate and the combined organics were dried (Na2SO4) and evaporated. Distillation under vacuum removed most of the remaining diglyme. The residue was purified by column chromatography (light petroleum:diethyl ether 2:1) to give a clear oil which crystallised on standing to give the title compound as white needles. 13C NMR (CDCl3): δ 25.7, 25.7, 32.6, 39.1, 62.9, 74.3, 125.7, 127.2, 129.5, 129.7, 132.1, 133.2, 133.7, 137.5, 138.7 and 144.6.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560597B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-b8c3fa2dbf1b481391b010440c8960b9
Quellennotizuspto-grants-2009_07