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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2263591생성일: 2026년 10월 26일

Ammonia → (2-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethynyl)triisopropylsilane

https://huagongshe.com/reaction/2263591

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Ammonium ChlorideHCID 25517—
반응물Lithium ChlorideHCID 433294—
반응물4-Bromo-2-(bromomethyl)-1-chlorobenzeneHCID 11558280—
반응물((4-Iodophenyl)ethynyl)triisopropylsilaneHCID 57809611—
반응물HCID 178418546HCID 178418546—
반응물HCID 178418918HCID 178418918—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(2-(4-(5-Bromo-2-chlorobenzyl)phenyl)ethynyl)triisopropylsilaneHCID 16065644—

반응 조건

온도-25 °C

반응 단계

Under argon 0.66 ml of a 2 M solution of isopropylmagnesium chloride in tetrahydrofuran are added dropwise to a solution of 0.50 g (4-iodo-phenylethynyl)-triisopropyl-silane in 2.2 ml dry tetrahydrofuran chilled to −25° C. The solution is stirred for 30 min at −25° C. and then combined with 0.26 ml of a 1 M solution of CuCN*2 LiCl in tetrahydrofuran (prepared by dissolving CuCN and LiCl in the ratio 1:2). Shortly afterwards, 0.35 g 4-bromo-2-bromomethyl-1-chlorbenzene are added and the reaction mixture is brought up to −5° C. in the cooling bath. After 6 h stirring at −5° C. the solution is heated to ambient temperature and stirred overnight. Then a mixture of saturated ammonium chloride solution and 25% ammonia solution (9:1) is added and the resulting mixture is added to water. The organic phase is separated off and the aqueous phase is extracted with ethyl acetate, the combined organic phases are dried over sodium sulphate, and the solvent is removed. The residue is purified through silica gel (cyclohexane).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07851602B2
출처 데이터셋uspto-grants-2010_12
ORD IDord-35aa149ddade45e3893d93659cc0962b
출처 메모uspto-grants-2010_12