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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 862069생성일: 2026년 10월 25일

Water → (4-Methoxymethoxy-phenylethynyl)-trimethylsilane

https://huagongshe.com/reaction/862069

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-(2,2-Dibromoethenyl)phenol methoxymethyl etherHCID 54096825—
반응물HCID 178418244HCID 178418244—
용매TetrahydrofuranHCID 8028—
생성물(4-Methoxymethoxy-phenylethynyl)-trimethylsilaneHCID 10657368—

반응 단계

A solution of 4-(2,2-dibromoethenyl)phenol methoxymethyl ether (16.56 g) in THF (350 ml) was cooled to -78° C., to which was added dropwise, under argon atmosphere, a 1.6M n-butyl lithium hexane solution (70 ml). The mixture was stirred for one hour under the same conditions, which was then warmed and stirred for one hour at room temperature. The reaction mixture was cooled with ice, to which was added dropwise trimethylchlorosilane (7.2 ml). The mixture was then stirred for 3 hours while warming up to room temperature, to which was added water to quench the reaction, followed by extraction with ethyl acetate. The organic layer was washed (a saturated aqueous saline solution) and dried (anhydrous magnesium sulfate), then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluted with ethyl acetate/hexane) to give 4-(2-trimethylsilylethynyl)phenol methoxymethyl ether (10.76 g) (Compound B-26). The physical properties are shown in Table 8.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05716971
출처 데이터셋uspto-grants-1998_02
ORD IDord-6b044bd90cf64d54978473a34cffc4cc
출처 메모uspto-grants-1998_02