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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1592717생성일: 2026년 10월 27일

Imidazole → (5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane

https://huagongshe.com/reaction/1592717

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물tert-Butyldimethylsilyl chlorideHCID 28928—
반응물1-(2-Bromophenyl)ethan-1-olHCID 6950331—
생성물(5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silaneHCID 12546529582%

반응 단계

To a 25 mL flask containing (S)-(−)-2-bromo-alpha-methylbenzyl alcohol (200 mg, 1.0 mmol), tert-butyldimethylsilyl chloride (165 mg, 1.1 mmol), and imidazole (203 mg, 3.0 mmol) flushed with nitrogen was added 5 mL of dimethylformamide. After stirring overnight, the mixture was quenched with saturated sodium bicarbonate, diluted with ethyl acetate, washed with NaH2PO4, saturated aqueous sodium bicarbonate, water, brine, dried (Na2SO4), filtered, and concentrated. Purification by flash chromatography (10 g SiO2, linear gradient 0-10% ethyl acetate/Hexanes, 30 mL/minute, over 30 minutes) gave about 260 mg (0.82 mmol, 82%) of (5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane as a colorless oil. GC/MS (EI): 315 (M). The (5)-[1-(2-Bromo-phenyl)-ethoxy]-tert-butyl-dimethyl-silane was coupled to piperazine in a manner similar to Preparation 1A. LRMS (ESI+): 321.5 (M+1)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07291619B2
출처 데이터셋uspto-grants-2007_11
ORD IDord-68095268d655410ea896a566a67e6eeb
출처 메모uspto-grants-2007_11