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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 602739생성일: 2026년 10월 24일

2-Cyclohexen-1-one → Benzenesulfonyl-(3-oxo-cyclohexyl)-acetic acid methyl ester

https://huagongshe.com/ko/reaction/602739

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyclohexen-1-oneHCID 13594—
반응물Methyl phenylsulfonyl acetateHCID 555619—
반응물Sodium MethoxideHCID 10942334—
용매MethanolHCID 887—
용매Ammonium ChlorideHCID 25517—
생성물Benzenesulfonyl-(3-oxo-cyclohexyl)-acetic acid methyl esterHCID 11088194185.3%

반응 단계

To a stirred solution of 9 g (0.042 mol) of methyl phenylsulfonylacetate in 90 mL of MeOH at 0° C., 1.56 mL (0.008 mol, 0.2 eq) of a solution of sodium methoxide (5.4 M in MeOH) were added. After 15 min, 4.04 g (0.02 mol) of 2-cyclohexen-1-one were added. The reaction mixture was allowed to reach RT within 4 hours, diluted with saturated aqueous NH4Cl and extracted with EtOAc. The combined organic phases were dried over Na2SO4, filtered and evaporated. Column chromatography on silica gel with heptane/EtOAc 1:1 yielded 11.50 g (88%) of benzenesulfonyl-(3-oxo-cyclohexyl)-acetic acid methyl ester as a racemic mixture of diastereomers, light yellow oil, MS: 311 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07906546B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-d8e4ad3210554545a8daec50eaff5962
출처 메모uspto-grants-2011_03