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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 59205생성일: 2026년 10월 24일

Imidazole → (4-(5-Bromo-2-chlorobenzyl)phenoxy)(tert-butyl)dimethylsilane

https://huagongshe.com/ko/reaction/59205

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물4-((5-Bromo-2-chlorophenyl)methyl)phenolHCID 57423751—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매DimethylformamideHCID 6228—
생성물(4-(5-Bromo-2-chlorobenzyl)phenoxy)(tert-butyl)dimethylsilaneHCID 5974770299.4%

반응 단계

To a solution of 4-(5-bromo-2-chloro-benzyl)-phenol (9.01 g, 30.28 mmol) dissolved in N,N-dimethylformamide (100 mL) and cooled to 0 degrees Celsius (ice bath) was added imidazole (4.53 g, 66.6 mmol) and 4-dimethylaminopyridine (370 mg, 3.03 mmol). tert-butylchlorodimethylsilane (6.85 g, 45.4 mmol) was added and the ice bath was removed. The reaction mixture was allowed to stir at room temperature overnight (˜16 hours), water (400 mL) was added and the resulting mixture was extracted with ethyl acetate (200 mL). The aqueous layer was extracted two additional times with ethyl acetate (200 mL). The combined organic layers were washed with water (200 mL), brine (200 mL), dried over sodium sulfate, filtered and concentrated under reduced pressure. The crude material was purified by flash chromatography over silica gel using the ISCO automated chromatography unit (120 g silica gel column) and eluting with a gradient of 0 to 50% ethyl acetate in heptane. 12.4 g (99% yield) of product obtained as a clear oil. 1H NMR (400 MHz, CHLOROFORM-d) delta ppm 0.18 (s, 6 H), 0.97 (s, 9 H), 3.96 (s, 2 H), 6.77 (d, J=8.4 Hz, 2 H), 7.01 (d, J=8.4 Hz, 2 H), 7.17-7.30 (m, 3 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09439902B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-772f0388c67e476eac87874a10230aca
출처 메모uspto-grants-2016_09