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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 512019생성일: 2026년 10월 24일

Saccharin → N-(6-tert-Butyldimethylsilyloxy-hexyl)saccharin

https://huagongshe.com/ko/reaction/512019

반응식

참여 물질

역할이름HCID투입량
반응물SaccharinHCID 5143—
반응물Sodium hydrideHCID 24758—
반응물(6-Bromohexyloxy)-tert-butyldimethylsilaneHCID 4260352—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(6-tert-Butyldimethylsilyloxy-hexyl)saccharinHCID 2501886845%

반응 단계

To a solution of saccharin (92 mg, 0.5 mmol) in anhydrous DMF (4 mL), at room temperature, under a nitrogen atmosphere, was added NaH (60% dispersion in mineral oil, 21 mg, 0.52 mmol). The mixture was stirred at the same temperature for additional 15 min, a solution of (6-bromohexyloxy)-tert-butyldimethylsilane (177 mg, 0.6 mmol) in DMF (1 mL) was added and the resulting mixture microwaved at 150° C. for 10 min. The reaction mixture was cooled to room temperature and diluted with water (5 mL) and AcOEt (10 mL). The organic layer was separated and the aqueous layer extracted with AcOEt (2×10 mL). The combined organic layer was washed with brine, dried (MgSO4) and the solvent removed in vacuum. The residue was purified by flash column chromatography on silica gel (20% ethyl acetate-petroleum ether) to give 83.8 (89 mg, 45% yield), as a viscous liquid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09102622B2
출처 데이터셋uspto-grants-2015_08
ORD IDord-b27bcf4747144841a9e1fa95fccda40d
출처 메모uspto-grants-2015_08