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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1518951Erstellt: 27. Oktober 2026

Sodium Carbonate → (R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamide

https://huagongshe.com/reaction/1518951

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium CarbonateHCID 10340—
EduktTriethylsilaneHCID 12052—
EduktN-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 28560458—
EduktHCID 178418416HCID 178418416—
LösungsmittelDimethylformamideHCID 6228—
Produkt(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamideHCID 86691231—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

Mix N-[(1R)-1-(4-bromophenyl)ethyl]-methanesulfonamide (10 g, 35 mmol), (1,1′-bis(diphenylphosphino)-ferrocene)palladium(II) chloride (733 mg, 0.9 mmol), sodium carbonate (3.81 g, 35 mmol) and DMF (50 mL) in a 300 mL PARR reactor. Add triethylsilane (11.6 mL, 0.72 mmol) and purge the reactor with carbon monoxide three times. Then charge the reactor with carbon monoxide (50 psi) and stir the mixture at 90° C. for 15 hours. Cool the reactor to ambient temperature, filter over Celite® pad and wash with DCM (150 mL). Sequentially wash the filtrate with water then brine (2×80 mL). Concentrate the organic filtrate under vacuum to obtain the residue as an orange oil. Purify the crude by silica gel flash chromatography eluting with hexane/ethyl acetate (0 to 30% ethyl acetate) to provide the title compound (5.6 g, 70%, ee>98%). MS (m/z): 228 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09073856B2
Quelldatensatzuspto-grants-2015_07
ORD IDord-948b7050c31d4a639642eafa35ff2efa
Quellennotizuspto-grants-2015_07