戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 84470作成日:2026年10月26日

Potassium Carbonate → 4,5-Dihydrobenzo[b]thieno[2,3-d]oxepine

https://huagongshe.com/reaction/84470

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物3-(2-(2-Iodophenoxy)ethyl)thiopheneHCID 64084785—
触媒Tetraethylammonium ChlorideHCID 5946—
触媒palladium(II) acetateHCID 167845—
溶媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物4,5-Dihydrobenzo[b]thieno[2,3-d]oxepineHCID 57900155—

反応手順

To a stirred solution of 2-iodophenol (6.7 g, 30.6 mmol), 2-(3-thienyl)ethanol (3.57 g, 27.8 mol) and triphenylphosphene (8.00 g, 30.6 mmol) in THF, was slowly added a solution of DEAD (4.8 ml, 30.6 mmol). Reaction mixture was stirred at room temperature for 3 hours. Purification on silica gave 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene. A mixture of 3-[2-(2-iodo-phenoxy)-ethyl]-thiophene (1.55 g, 4.69 mmol), palladium(II) acetate (105 mg, 0.47 mmol), potassium carbonate (3.2 g, 23.45 mmol), triphenylphosphene (246 mg, 0.94 mmol) and tetraethylammonium chloride (1.3 g, 4.69 mmol) in DMF was microwaved at 100° C. for 1 hour. The reaction was diluted with dichloromethane and filtered through celite. The filtrate was washed with water, dried (MgSO4), and concentrated in-vacuo. Purification on silica gave 4,5-dihydrobenzo[b]thieno[2,3-d]oxepine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846762B2
出典データセットuspto-grants-2014_09
ORD IDord-7923b99daeb74876aea1a1cb1e406144
出典メモuspto-grants-2014_09