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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 747079생성일: 2026년 10월 25일

Benzene, 2-bromo-1,4-dimethyl- → (2,5-Dimethylphenyl)(dimethyl)octylsilane

https://huagongshe.com/reaction/747079

반응식

참여 물질

역할이름HCID투입량
반응물Benzene, 2-bromo-1,4-dimethyl-HCID 11121—
반응물Ammonium ChlorideHCID 25517—
반응물ChlorodimethyloctylsilaneHCID 87482—
반응물MagnesiumHCID 5462224—
용매TetrahydrofuranHCID 8028—
생성물(2,5-Dimethylphenyl)(dimethyl)octylsilaneHCID 5873848342.7%

반응 조건

온도70 °C

반응 단계

1.95 g (80.2 mmol) of finely cut magnesium metal was placed in a 200 ml four-necked flask, and 50 ml of anhydrous tetrahydrofuran was further charged. The mixture was heated up to 70° C. while stirring, and 50 ml of a solution of 5 g (27.0 mmol) of 2-bromo p-xylene in anhydrous tetrahydrofuran was added dropwise while caring for steep reaction (reflux). After completion of the addition, it was refluxed for 30 minutes, then, cooled to 40° C., and to this was added 6.7 g (32.4 mmol) of dimethyloctylsilyl chloride while stirring. The solution was again heated and refluxed for 3 hours. The reaction mixture was charged in an aqueous saturated ammonium chloride solution, and extracted (toluene/water) and the organic phase was dried over sodium sulfate. After concentration, the product was purified and isolated by silica gel column chromatography (n-hexane) to obtain 3.19 g of 2-(dimethyloctylsilyl)-p-xylene.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07396571B2
출처 데이터셋uspto-grants-2008_07
ORD IDord-81637682aa414a1891c98ee78018a83c
출처 메모uspto-grants-2008_07