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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1483024Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1483024

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); seal; and stir the mixture at 90° C. for 15 hours. Cool the reactor to ambient temperature; filter the resulting mixture over Celite® pad; and wash the pad with DCM (150 mL). Collect the filtrate and sequentially wash the filtrate with water then brine (2×80 mL). Concentrate the organic filtrate under reduced pressure to obtain the residue as an orange oil. Purify 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
PatentnummerUS09416138B2
Quelldatensatzuspto-grants-2016_08
ORD IDord-77e918318dff4ba7a06fb4c1fea5dc27
Quellennotizuspto-grants-2016_08