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HRID 13231作成日:2026年10月24日

Dichloromethane → 2-Ethynyl-4-methyl-phenol

https://huagongshe.com/ja/reaction/13231

反応式

関与物質

役割名称HCID仕込み量
反応物DichloromethaneHCID 6344—
反応物2-Bromo-4-methylphenolHCID 23109—
反応物TrimethylsilylacetyleneHCID 66111—
反応物Potassium FluorideHCID 522689—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418476HCID 178418476—
溶媒HCID 68453242HCID 68453242—
生成物2-Ethynyl-4-methyl-phenolHCID 10486892—

反応手順

A flask is flushed with N2 and charged with 2-Bromo-4-methylphenol (20 mmol) and dissolved in 1/1 Et3N/dioxane. Bis(triphenylphosphine)palladium(II) dichloride (PdCl2(PPh3)2) (0.2 mmol) is added, followed by 0.4 mmol of CuI. Trimethylsilylacetylene (24 mmol) is added drop-wise to the reaction mixture. The reaction mixture is stirred overnight under N2. The solvents are removed under vacuum and the resulting liquid is extracted by washing with ethyl ether. The ethyl ether extracts are combined and washed with H2O, then dried over anhydrous sodium sulfate. The solvent was removed under vacuum and the product is purified by column chromatography. The purified product is placed in a N2-flushed flask and dissolved in methanol. Potassium fluoride (65 mmol) is added and the reaction stirred under a N2 blanket for 16 h. The reaction mixture is poured into CH2Cl2 and extracted with H2O, then dried over Na2SO4, filtered and the solvent is removed under vacuum. The resulting product is purified by column chromatography to yield 2-ethynyl-4-methyl-phenol (3).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728051B2
出典データセットuspto-grants-2010_06
ORD IDord-05b116f3a02a429f932af61225491e18
出典メモuspto-grants-2010_06