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HRID 22192作成日:2026年10月24日

2-Fluorothiophenol → Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate

https://huagongshe.com/ja/reaction/22192

反応式

関与物質

役割名称HCID仕込み量
反応物2-FluorothiophenolHCID 520216—
反応物Sodium ethoxideHCID 2723922—
反応物Ethyl 2-(4-fluorophenyl)acrylateHCID 19736751—
溶媒EthanolHCID 702—
生成物Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetateHCID 1992755282.2%

反応手順

The crude product from Step A (3.9 g, 20 mole) was taken up in 20 ml of ethanol. To this solution, being stirred at room temperature, was added 2-fluorothiophenol (2.5 g, 20 mmole) and 50 mg of solid sodium ethoxide. After stirring for eight hours the ethanol was concentrated and the residue taken up in ether. The ether mixture was washed twice with 15% NaOH solution, dried (MgSO4) and concentrated to a colorless oil (5.3 g, 82% yield). 1H NMR (CDCl3) δ: 7.28 (4H, m), 7.06 (4H, m), 4.13 (2H, m), 3.72 (1H, m), 3.55 (1H, m), 3.20 (1H, dd, J=6, 12 Hz), 1.21 (3H, t, J=6 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05428027
出典データセットuspto-grants-1995_06
ORD IDord-c5b877e7aced48708173e5628ebd3f82
出典メモuspto-grants-1995_06