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HRID 1794507作成日:2026年10月26日

2-(2,5-Dimethoxy-phenyl)-1-(4-methoxy-phenyl)ethanone → 2-(4-Hydroxy-phenyl)benzofuran-5-OL

https://huagongshe.com/reaction/1794507

反応式

関与物質

役割名称HCID仕込み量
反応物2-(2,5-Dimethoxy-phenyl)-1-(4-methoxy-phenyl)ethanoneHCID 358216—
反応物Pyridinium chlorideHCID 10176127—
溶媒WaterHCID 962—
生成物2-(4-Hydroxy-phenyl)benzofuran-5-OLHCID 65693651%

反応条件

温度200 °C

反応手順

A mixture of 74 (1.5 g, 5.2 mmol) and Pyridine HCl (10 g) was heated to 200° C. After 1.5 hr, the reaction was cooled and diluted with water. The aqueous layer was extracted with EtOAc and the organic layer was dried, concentrated to give a solid which was triturated with CH2Cl2 to give a solid (0.6 g, 51%): Mp=275–278° C.; 1H NMR (DMSO-d6) δ 9.81 (br s, 1 H), 9.12 (br s, 1 H), 7.66 (d, 2 H, J=2.5 Hz), 7.32 (d, 1 H, J=8.5 Hz), 7.00 (s, 1 H), 6.90–6.83 (m, 3 H), 6.65 (dd, 1 H, J=8.6 Hz, 2.6 Hz); MS 225 (M−H)−.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07022733B2
出典データセットuspto-grants-2006_04
ORD IDord-8f4f569ca48f43ba8ea62c03fde958a3
出典メモuspto-grants-2006_04