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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1980514생성일: 2026년 10월 25일

Isopropanol → Chloromethyl[bis(4-fluorophenyl)](2-propoxy)silane

https://huagongshe.com/reaction/1980514

반응식

참여 물질

역할이름HCID투입량
반응물IsopropanolHCID 3776—
반응물TriethylamineHCID 8471—
반응물1-Bromo-4-fluorobenzeneHCID 9993—
반응물Trichloro(chloromethyl)silaneHCID 15258—
반응물ChlorosilaneHCID 61622—
반응물MagnesiumHCID 5462224—
촉매IodineHCID 807—
용매Diethyl EtherHCID 3283—
생성물Chloromethyl[bis(4-fluorophenyl)](2-propoxy)silaneHCID 1339240243%

반응 단계

A mixture of 23.2 g (0.955 mol) of magnesium and 50 mg of iodine in 200 ml of ether was stirred while a solution of 167 g (0.954 mol) of 4-bromofluorobenzene in 600 ml of ether was added at a rate that maintained gentle reflux. After another 2 hours at reflux, the solution was cooled in ice and stirred while a solution of 40 ml (0.32 mol) of chloromethyltrichlorosilane in ether was added dropwise over 40 minutes. The resulting mixture was stirred at room temperature for 17 hours, chilled in ice, treated with 24 ml of isopropanol), stirred another 10 minutes, and filtered. The filtrate was concentrated to a gummy solid, hexanes was added, the resulting slurry was filtered, and the hexanes filtrate was evaporated to leave an oil. Analysis by nmr showed the presence of unreacted chlorosilane, so the oil was dissolved in hexanes containing 30 ml of isopropanol, and the solution was chilled in ice and treated with a solution of 42 ml (0.30 mol) of triethylamine in hexanes. The resulting slurry was stirred at room temperature for 3 hours and filtered, and the filtrate was evaporated to leave an oil. Distillation provided 44.8 g (43%) of the title compound as a colorless liquid: bp 120°-140° (0.1 mm); nD22 1.5211; nmr (CDCl3) 1.2 (6H, d), 3.2 (2H, s), 4.1 (1H, septet), 7.1 (4H, t), 7.7 (4H, d of d).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04510136
출처 데이터셋uspto-grants-1985_04
ORD IDord-1d661dbc817541bf9158171c8f20da0e
출처 메모uspto-grants-1985_04