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HRID 230847作成日:2026年10月27日

Methyltriphenylphosphonium iodide → N-(5-Chloro-3-methylidene-2,3-dihydro-1-benzofuran-4-yl)-2,2,2-trifluoroacetamide

https://huagongshe.com/reaction/230847

反応式

関与物質

役割名称HCID仕込み量
反応物Methyltriphenylphosphonium iodideHCID 638159—
反応物Potassium tert-butoxideHCID 23665647—
反応物N-(5-Chloro-3-oxo-2,3-dihydro-1-benzofuran-4-yl)-2,2,2-trifluoroacetamideHCID 57763220—
溶媒TolueneHCID 1140—
生成物N-(5-Chloro-3-methylidene-2,3-dihydro-1-benzofuran-4-yl)-2,2,2-trifluoroacetamideHCID 57763270—

反応手順

To a mixture of potassium tert-butoxide (2.0) and methyltriphenylphosphonium iodide (7.1 g) was added dry toluene (70 ml) and the mixture stirred at room temperature for 30 min, then heated under reflux for 30 min. The mixture was cooled to room temperature, a solution of Intermediate 22 (1.0 g) in toluene (30 ml) added dropwise and the mixture heated under reflux for 30 min. The mixture was cooled and quenched by the dropwise addition of saturated ammonium chloride solution. The mixture was partitioned between ethyl acetate and water and the organic phase washed with water. The combined aqueous layers were re-extracted with ethyl acetate and the combined organic layers dried over sodium sulphate and concentrated in vacuo to give a dark brown oil. Purification by column chromatography on silica gel, eluting with 10% ethyl acetate in cyclohexane, gave the title compound as a rose coloured solid (0.5 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07566786B2
出典データセットuspto-grants-2009_07
ORD IDord-1368f349ddde440a9dc52c3212aec625
出典メモuspto-grants-2009_07