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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 965960Erstellt: 25. Oktober 2026

4-Bromo-N-methoxy-N-methylbenzamide → 1-Butanone, 1-(4-bromophenyl)-

https://huagongshe.com/reaction/965960

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Bromo-N-methoxy-N-methylbenzamideHCID 10999252—
EduktHCID 178455851HCID 178455851—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt1-Butanone, 1-(4-bromophenyl)-HCID 7868082,1%

Reaktionsschritte

To a solution of 4-bromo-N-methoxy-N-methylbenzamide (13.4 g, 54.2 mmol) in THF (200 ml) was added n-PrMgBr (2M THF solution, 54.0 ml, 108 mmol) at 0° C. The mixture was stirred at room temperature for 45 minutes. Further n-PrMgBr (13.5 ml, 27.0 mmol) was added at 0° C., and the mixture was stirred at room temperature for 30 minutes. The excess reagent was quenched with saturated aqueous NH4Cl (200 ml), and ether (300 ml) was added. The organic layer was separated and the aqueous layer was extracted with ether (300 ml). The combined organic layer was washed with water (200 ml) and brine (200 ml), dried over Na2SO4, and concentrated in vacuo. The obtained residue was chromatographed on a column of silica gel eluting with hexane/ethyl acetate (15:1) to give 10.1 g (82%) of the title compound as a yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06951876B2
Quelldatensatzuspto-grants-2005_10
ORD IDord-18dc0014c15a4c96b72c12622aae81c7
Quellennotizuspto-grants-2005_10