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HRID 602739作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物2-Cyclohexen-1-oneHCID 13594—
反応物Methyl phenylsulfonyl acetateHCID 555619—
反応物Sodium MethoxideHCID 10942334—
溶媒MethanolHCID 887—
溶媒Ammonium ChlorideHCID 25517—
生成物Benzenesulfonyl-(3-oxo-cyclohexyl)-acetic acid methyl esterHCID 11088194185.3%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07906546B2
出典データセットuspto-grants-2011_03
ORD IDord-d8e4ad3210554545a8daec50eaff5962
出典メモuspto-grants-2011_03