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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1483024생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/1483024

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); 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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09416138B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-77e918318dff4ba7a06fb4c1fea5dc27
출처 메모uspto-grants-2016_08