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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 46313생성일: 2026년 10월 23일

Imidazole → Tert-butyl(4-chloro-2-iodophenoxy)dimethylsilane

https://huagongshe.com/ko/reaction/46313

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물4-Chloro-2-iodophenolHCID 620234—
용매DichloromethaneHCID 6344—
생성물Tert-butyl(4-chloro-2-iodophenoxy)dimethylsilaneHCID 5943649395%

반응 단계

To a solution of 4-chloro-2-iodophenol (1.587 g, 6.238 mmol) in dichloromethane (10 ml) was added 1H-imidazole (1.01 g, 14.3 mmol) followed by a solution of tert-butyl(chloro)dimethylsilane (2.63 ml, 13.7 mmol) in dichloromethane (10 ml) dropwise. The resulting white suspension was stirred for 16 hours at room temperature before concentrating in vacuo. The residue was diluted with ethyl acetate (20 ml) and water (20 ml). The aqueous phase was acidified with hydrochloric acid (2 M aqueous solution) and extracted with ethyl acetate. The combined organic layers were washed with hydrochloric acid (2 M aqueous solution), saturated aqueous sodium chloride solution, dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography (40 g silica gel column) eluting with ethyl acetate:heptane (gradient 0:1 to 3:7, by volume) to afford the title compound as pale yellow oil, 2.2 g, 95% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541588B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-4d4a267f774a4da2b27239b1459333d4
출처 메모uspto-grants-2013_09