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HRID 351428作成日:2026年10月26日

Potassium Hydroxide → 4'-Benzyloxyphenyl acetylene

https://huagongshe.com/reaction/351428

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium HydroxideHCID 14797—
反応物TrimethylsilylacetyleneHCID 66111—
反応物1-(Benzyloxy)-4-iodobenzeneHCID 519671—
触媒HCID 178418476HCID 178418476—
溶媒DiethylamineHCID 8021—
生成物4'-Benzyloxyphenyl acetyleneHCID 1490323—

反応条件

温度25 °C

反応手順

4-benzyloxy iodobenzene (193 g, 0.625 mol), ethynyl-trimethyl-silane (75 g, 0.76 mol), Cul (2 g, 10.5 mmol) and Pd(PPh3)2Cl2 (1 g, 1.0 mmol) were added to diethylamine (880 mL) at 0° C. The reaction mixture was warmed to 25° C. and then stirred for 6 h. The reaction mixture was concentrated and partitioned in H2O/ethyl acetate (100 mL/100 mL). The reaction mixture was further extracted with ethyl acetate (300 mL×2). The combined organic layers were washed by water (300 mL), dried over MgSO4 and concentrated in vacuo. The crude product was dissolved in methanol (400 mL) and was stirred with KOH (28 g, 0.5 mol) for 1 h at 25° C. Concentration and purification by silica gel column chromatograph (5% ethyl acetate/Hexane) yielded 4-benzyloxy phenyl acetylene as liquid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07183445B2
出典データセットuspto-grants-2007_02
ORD IDord-7f0bafc984b14b18824e44153f5ddef6
出典メモuspto-grants-2007_02