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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 14454생성일: 2026년 10월 26일

Chlorotrimethylsilane → Ethanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-

https://huagongshe.com/reaction/14454

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물BromineHCID 24408—
반응물1-(2,2-Dimethyl-2,4-dihydro-1,3-benzodioxin-6-yl)ethan-1-oneHCID 21880610—
반응물Sodium hexamethyidisilazaneHCID 45051731—
용매TetrahydrofuranHCID 8028—
생성물Ethanone, 2-bromo-1-(2,2-dimethyl-4H-1,3-benzodioxin-6-yl)-HCID 11150315—

반응 단계

To the product of step (b) (23.4 g, 0.113 mol) in 600 mL of THF at −78° C. was added 135 mL of 1.0 M sodium hexamethyldisilazane in THF (Sigma-Aldrich). After 1 hour, trimethylsilyl chloride (15.8 mL, 0.124 mol) was added. After another 30 minutes, bromine (5.82 mL, 0.113 mol) was added. After 10 minutes, the reaction was quenched by diluting the reaction mixture with diethyl ether and pouring it onto 500 mL of 5% aqueous Na2SO3 premixed with 500 mL of 5% aqueous NaHCO3. The phases were separated and the organic phase was washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to give the title compound as an oil that solidified upon storage in the freezer.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07732441B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-ef4ea43a78ff495cb8c3230a83042d2f
출처 메모uspto-grants-2010_06