戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 24297作成日:2026年10月23日

2-Methylbenzenesulfonic acid → Dithiophenylacetic Acid, 2-(2-pyridinyl)ethyl Ester

https://huagongshe.com/ja/reaction/24297

反応式

関与物質

役割名称HCID仕込み量
反応物2-Methylbenzenesulfonic acidHCID 6925—
反応物2-VinylpyridineHCID 7521—
反応物Di(2-thienyl)acetic acidHCID 20443—
溶媒BenzeneHCID 241—
生成物Dithiophenylacetic Acid, 2-(2-pyridinyl)ethyl EsterHCID 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. 1H NMR (CDCl3) δ=3.042 (t, 2 H), δ=3.573 (t, 2 H), δ=4.233 (s, 2H ) δ=6.968-7.476 (m, 8H), δ=8.467, (d, 1H). 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06855840B2
出典データセットuspto-grants-2005_02
ORD IDord-c38a814f41cc4b92a236e4eefc635c9c
出典メモuspto-grants-2005_02