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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 880225Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/880225

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

Combine 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. Charge the reactor with carbon monoxide (50 psi) and stir the mixture at 90° C. for 15 h. Cool the reactor to ambient temperature; open; filter mixture through a Celite® pad; and wash the pad with DCM (150 mL). Sequentially wash the filtrate with water then brine (2×80 mL). Concentrate the organic phase under reduced pressure to obtain the residue as an orange oil. Purify the orange oil by silica gel flash chromatography eluting with hexane/EtOAc (0 to 30% EtOAc) 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
PatentnummerUS08993568B2
Quelldatensatzuspto-grants-2015_03
ORD IDord-e84f96b910b44827b4ff26260fbc4ed5
Quellennotizuspto-grants-2015_03