돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2038216생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/2038216

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamideHCID 28560458—
반응물HCID 178418416HCID 178418416—
촉매TriethylsilaneHCID 12052—
용매DimethylformamideHCID 6228—
생성물(R)-N-(1-(4-formylphenyl)ethyl)methanesulfonamideHCID 8669123170.4%

반응 단계

Charge a 300 mL PARR reactor with 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). Add triethylsilane (11.6 mL, 0.72 mmol) and purge the reactor with carbon monoxide three times. Pressurize the PARR reactor with carbon monoxide (50 psi) and stir the mixture at 90° C. for 15 hours. Cool the reactor to ambient temperature; filter through 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 provide an orange oil residue. Purify the residue by silica gel flash chromatography eluting with hexane/EtOAc (0 to 30% EtAc) 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 번호US08575352B2
출처 데이터셋uspto-grants-2013_11
ORD IDord-f3bde30ae8e64a0fbe61c42f787704c8
출처 메모uspto-grants-2013_11