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HRID 28509作成日:2026年10月25日

Methyl (methylsulfinyl)methyl sulfide → 2-Chloro-1-methoxy-3-[2-(methylsulfanyl)-2-(methylsulfinyl)vinyl]benzene

https://huagongshe.com/reaction/28509

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl (methylsulfinyl)methyl sulfideHCID 99129—
反応物2-Chloro-3-methoxybenzaldehydeHCID 12575695—
溶媒TetrahydrofuranHCID 8028—
生成物2-Chloro-1-methoxy-3-[2-(methylsulfanyl)-2-(methylsulfinyl)vinyl]benzeneHCID 8659650848%

反応手順

To a solution of 2-chloro-3-methoxybenzaldehyde 7a (4.65 g, 27.3 mmol) and methyl (methylthio)methyl sulfoxide (4.3 mL, 43.9 mmol) in THF (25 mL) was added a 40% methanolic solution of Triton B (6.2 mL, 13.6 mmol) and the resulting solution was refluxed for 16 hours. After THF was removed, the residue was taken up in ethyl acetate,washed with 1 N HCl, H2O, and brine, then was dried over Na2SO4, and concentrated. Purification by column chromatography on silica gel with dichloromethane afforded 2-chloro-1-methoxy-3-[2-methylsulfanyl)-2-(methylsulfinyl)vinyl]benzene 7b (3.61 g, 48%) as a yellow oil. GCMS (EI) m/z 225 (M+-Cl16), 210 (M+-Cl-OMe).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07419983B2
出典データセットuspto-grants-2008_09
ORD IDord-16169f1d72cb421ba0df70e5d7011029
出典メモuspto-grants-2008_09