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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 351428생성일: 2026년 10월 25일

Potassium Hydroxide → 4'-Benzyloxyphenyl acetylene

https://huagongshe.com/reaction/351428

반응식

참여 물질

역할이름HCID투입량
반응물Potassium HydroxideHCID 14797—
반응물TrimethylsilylacetyleneHCID 66111—
반응물1-(Benzyloxy)-4-iodobenzeneHCID 519671—
촉매HCID 178418476HCID 178418476—
용매DiethylamineHCID 8021—
생성물4'-Benzyloxyphenyl acetyleneHCID 1490323—

반응 조건

온도25 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07183445B2
출처 데이터셋uspto-grants-2007_02
ORD IDord-7f0bafc984b14b18824e44153f5ddef6
출처 메모uspto-grants-2007_02