関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 2-Methylbenzenesulfonic acid | HCID 6925 | — |
| 反応物 | 2-Vinylpyridine | HCID 7521 | — |
| 反応物 | Di(2-thienyl)acetic acid | HCID 20443 | — |
| 溶媒 | Benzene | HCID 241 | — |
| 生成物 | Dithiophenylacetic Acid, 2-(2-pyridinyl)ethyl Ester | HCID 86589915 | — |
反応手順
The crude product of newly synthesized dithiophenyl acetic acid (10 g, 59 mmol theoretically), freshly distilled 2-vinylpyridine (6.25 g, 59 mmol), and 1 mol % toluene sulfonic acid were dissolved in benzene and placed in a round bottom flask equipped with a vigreaux column and magnetic stirbar. The reaction was then heated to reflux and allowed to react for 16 hours. The viscous liquid that remained after the solvent was removed was then purified by column chromatography (silica 2/1 v/v hexane/ethyl acetate). Yield=3.9 g. 1 H NMR (CDCl3) δ=3.042 (t, 2 H), δ=3.573 (t, 2 H), δ=4.233 (s, 2 H) δ=6.968-7.476 (m, 8 H), δ=8.467, (d, 1 H). 13C NMR (CDCl3) δ=35.627 (CH2), δ=36.180 (CH2), δ=58.323 (CH2), δ=121.932 (CH), δ=123.383 (CH2), δ=127.501 (CH), δ=128.818 (CH), δ=129.346 (CH), δ=137.272 (C), δ=149.668 (CH), δ=159.305 (C), δ=235.369 (C═S).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07402690B2 |
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| 出典データセット | uspto-grants-2008_07 |
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| ORD ID | ord-3f9df8f224f845128c7ad2679ab28b3f |
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| 出典メモ | uspto-grants-2008_07 |
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