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HRID 1352722생성일: 2026년 10월 27일

Potassium Carbonate → 1-Bromo-3-(2-triisopropylsilyloxy-ethoxy)-naphtalene

https://huagongshe.com/reaction/1352722

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Bromo-2-naphtholHCID 12115596—
반응물Silane, (2-bromoethoxy)tris(1-methylethyl)-HCID 12137438—
촉매Tetrabutylammonium IodideHCID 67553—
용매DimethylformamideHCID 6228—
생성물1-Bromo-3-(2-triisopropylsilyloxy-ethoxy)-naphtaleneHCID 12115597—

반응 단계

A stirred mixture of 4.38 g (19.6 mmol) of 1-bromo-naphtalen-3-ol (prepared according to the procedure of M. S. Newman, V. Sankaran, D. R. Olson, J. Am. Chem. Soc. 1976, 98, 3237–3242), 5.52 g (19.6 mmol) of 1-bromo-2-triisopropylsilyloxy-ethane, 13.56 g (98.1 mmol) of potassium carbonate and 1.45 g (3.9 mmol) of tetrabutylammonium iodide in 50 mL of dimethylformamide is heated to 60° C. for 4 hours. Then an additional 0.55 g (2.0 mmol) of 1-bromo-2-triisopropylsilyloxy-ethane are added and stirring is continued for another hour at 60° C., after which TLC analysis indicated complete consumption of 1-bromo-naphtalen-3-ol. The mixture is allowed to cool to room temperature and brine is added. The resulting solution is extracted with ethyl acetate. The organic solution is washed twice with brine and the combined aqueous layers are back extracted with ethyl acetate. The organic layers are combined, dried, filtered and concentrated under reduced pressure. The oily brown residue is purified by column chromatography on silica gel (97.5:2.5 n-hexane/diethylether) to afford above title compound as a brown solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07220774B2
출처 데이터셋uspto-grants-2007_05
ORD IDord-4b0dad2faa5847a19ec25e20aa25fd92
출처 메모uspto-grants-2007_05