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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 880225생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/880225

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물TriethylsilaneHCID 12052—
반응물N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 28560458—
반응물HCID 178418416HCID 178418416—
용매DimethylformamideHCID 6228—
생성물(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamideHCID 86691231—

반응 조건

온도90 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08993568B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-e84f96b910b44827b4ff26260fbc4ed5
출처 메모uspto-grants-2015_03