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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1198675Erstellt: 25. Oktober 2026

Ethanol → [2'-(N-t-Butylsulfamoyl)-5'n-propylbiphenyl-4-yl]methanol

https://huagongshe.com/reaction/1198675

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktSodium HydroxideHCID 14798—
Edukt4-Bromobenzyl alcoholHCID 70119—
Edukt(2-(N-(tert-Butyl)sulfamoyl)-5-propylphenyl)boronic acidHCID 19939476—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelTolueneHCID 1140—
Produkt[2'-(N-t-Butylsulfamoyl)-5'n-propylbiphenyl-4-yl]methanolHCID 19939403—

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2.80 g (9.36 mmol ) of 2-(N-t-butylsulfamoyl)-5-n-propylphenylboronic acid (from Step B) and 4-bromobenzyl alcohol (5.25 g, 3 equiv) in toluene (125 mL) was added 1.25N NaOH (32 mL), EtOH (86 mL) and tetrakis(triphenylphosphine)palladium(0) (325 mg, 3 mol %). The mixture was stirred at 100° C. under N2 for 3 hours. The reaction was concentrated and the residue was extracted with ethyl acetate. The organic solution was washed with 1N NaOH, H2O and brine. Next, the organic phase was dried over anhydrous MgSO4 and concentrated in vacuo. The product was purified by flash chromatography, eluting with 2:1 hexane-EtOAc, to provide the titled compound; Rf =0.42 (1:1 EtOAc-hexane).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05281614
Quelldatensatzuspto-grants-1994_01
ORD IDord-9d06ee2337644cecb891377474571fe1
Quellennotizuspto-grants-1994_01