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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 13231생성일: 2026년 10월 24일

Dichloromethane → 2-Ethynyl-4-methyl-phenol

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

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물2-Bromo-4-methylphenolHCID 23109—
반응물TrimethylsilylacetyleneHCID 66111—
반응물Potassium FluorideHCID 522689—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
촉매HCID 178418476HCID 178418476—
용매HCID 68453242HCID 68453242—
생성물2-Ethynyl-4-methyl-phenolHCID 10486892—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728051B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-05b116f3a02a429f932af61225491e18
출처 메모uspto-grants-2010_06