돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1814335생성일: 2026년 10월 27일

Imidazole → (1-Bromo-naphthalen-2-yloxy)-triisopropyl-silane

https://huagongshe.com/reaction/1814335

반응식

참여 물질

역할이름HCID투입량
반응물ImidazoleHCID 795—
반응물PyridineHCID 1049—
반응물1-Bromo-2-naphtholHCID 11316—
반응물Triisopropylsilyl chlorideHCID 139400—
촉매4-(Dimethylamino)pyridineHCID 14284—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물(1-Bromo-naphthalen-2-yloxy)-triisopropyl-silaneHCID 2250424099.1%

반응 단계

1-Bromo-2-naphthol (5.00 g, 22.4 mmol) was mixed with triisopropylsilyl chloride (7.2 mL, 33.6 mmol), DMAP (402 mg, 3.30 mmol), imidazole (3.81 g, 56.0 mmol), and pyridine (6 mL) in CH2Cl2 (50 mL). The reaction was refluxed for two hours. TLC analysis (silica, 15% EtOAc-hexanes) indicated the reaction was complete. The reaction was allowed to cool to room temperature and then was diluted with H2O. The dilution was extracted three times with CH2Cl2. The organic extracts were combined, washed with brine solution, dried over Na2SO4, filtered through celite, and concentrated. The crude product was purified by flash chromatography (SiO2, 100% hexanes) to give (1-bromo-naphthalen-2-yloxy)-triisopropyl-silane (8.4 g, 22.2 mmol) as a colorless oil in 99% yield. 1H NMR (300 MHz) CDCl3 8.21 (d, J=7.5 Hz, 1H), 7.76 (d, J=8.5 Hz, 1H), 7.68 (d, J=8.8 Hz, 1H), 7.54 (m, 1H), 7.38 (m, 1H), 7.15 (d, J=8.8 Hz, 1H), 1.38 (m, 3H), 1.16 (d, J=7.1 Hz, 18H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06875765B2
출처 데이터셋uspto-grants-2005_04
ORD IDord-cc6ac67d4e814cdcaac13c3e119f2ed4
출처 메모uspto-grants-2005_04