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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 227620Erstellt: 24. Oktober 2026

4-Nitrobenzoyl chloride → 4-{[Tert-butyl(dimethyl)silyl]oxy}-1-(4-nitrophenyl)butan-1-one

https://huagongshe.com/de/reaction/227620

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Nitrobenzoyl chlorideHCID 8502—
EduktTert-butyl-(3-iodopropoxy)-dimethylsilaneHCID 11022956—
KatalysatorHCID 178418397HCID 178418397—
LösungsmittelBenzeneHCID 241—
LösungsmittelDimethylformamideHCID 6228—
Produkt4-{[Tert-butyl(dimethyl)silyl]oxy}-1-(4-nitrophenyl)butan-1-oneHCID 1160224647,5%

Reaktionsschritte

A mixture of Zn—Cu couple (2.68 g, 41.3 mmol) and tert-butyl(3-iodopropoxy)dimethylsilane (8.26 g, 27.5 mmol) in benzene (55 mL) and DMF (3.6 mL) was stirred vigorously at room temperature for 1 hour, heated to 60° C. for 4 hours, cooled to room temperature, and treated with a solution of 4-nitrobenzoyl chloride (3.4 g, 18.3 mmol) and (Ph3P)4Pd (0.847 g, 0.73 mmol) in benzene (36 mL) by cannula. The mixture was stirred for 1 hour, filtered through diatomaceous earth (Celite™), and partitioned between saturated NH4Cl and ethyl acetate. The aqueous phase was extracted three times with ethyl acetate and the combined extracts were washed with water and brine, dried (Na2SO4), filtered, and concentrated. The concentrate was purified by flash column chromatography on silica gel with 5% ethyl acetate/hexanes to provide 2.81 g of the desired product. MS(ESI(−)) m/e 322 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07560552B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-398a5d3424134113a4bd29f8ff47bc12
Quellennotizuspto-grants-2009_07