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HRID 2771作成日:2026年10月23日

Sodium Carbonate → 3-(2-Thienyl)pyridine

https://huagongshe.com/ja/reaction/2771

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物3-BromopyridineHCID 12286—
反応物2-Thiopheneboronic acidHCID 2733960—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物3-(2-Thienyl)pyridineHCID 59514516.3%

反応手順

A mixture of 3-bromopyridine (1.30 mL, 13.5 mmol) and tetrakis(triphenylphosphine) (0.468 g, 0.41 mmol) in 40 mL of dimethoxyethane is stirred under nitrogen at room temperature for 10 min. 2-Thiophene boronic acid (1.90 g, 14.8 mmol) and 20 mL of 1N sodium carbonate are added and the resulting mixture is refluxed overnight. The solution is cooled to room temperature and filtered through Celite. The filtrated is extracted with ether (2×30 mL). The combined organic layers are dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography eluting with a gradient of 10% EtOAc/hexanes to 20% EtOAc/hexanes to afford the title compound (0.355 g, 2.20 mmol) as a light yellow oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05731315
出典データセットuspto-grants-1998_03
ORD IDord-8d5d986597254a4b95b496e32a884a31
出典メモuspto-grants-1998_03