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2-Fluorothiophenol → Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Fluorothiophenol | HCID 520216 | — |
| 反応物 | Sodium ethoxide | HCID 2723922 | — |
| 反応物 | Ethyl 2-(4-fluorophenyl)acrylate | HCID 19736751 | — |
| 溶媒 | Ethanol | HCID 702 | — |
| 生成物 | Ethyl 4-fluoro-alpha-[[(2-fluorophenyl)thio]methyl]benzeneacetate | HCID 19927552 | 82.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05428027 |
| 出典データセット | uspto-grants-1995_06 |
| ORD ID | ord-c5b877e7aced48708173e5628ebd3f82 |
| 出典メモ | uspto-grants-1995_06 |