돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9254생성일: 2026년 10월 24일

Chlorotrimethylsilane → Ethyl 2-bromo-2-(pyridin-3-yl)acetate

https://huagongshe.com/ko/reaction/9254

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물N-bromobutanimideHCID 67184—
반응물Ethyl 3-pyridylacetateHCID 96490—
반응물Lithium HexamethyldisilazideHCID 2733832—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물Ethyl 2-bromo-2-(pyridin-3-yl)acetateHCID 21985933—

반응 조건

온도-78 °C

반응 단계

Ethyl 3-pyridylacetate (1.0 g, 1.0 eq) was dissolved in THF (50 mL) and cooled to −78° C. Lithium bis (trimethylsilyl) amide (6.66 mL, 1.1 eq) was added to the reaction and stirred for 20 minutes. Chlorotrimethylsilane (1.44 mL, 1.875 eq) was added at −78° C. and stirred for 20 minutes. N-bromosuccinimide (1.09 g, 1.01 eq) was added to the reaction mixture. The reaction mixture was allowed to stir and warm to room temperature overnight. The reaction mixture was diluted with H2O. The organic layer was extracted with ethyl acetate. The organic phase was dried over sodium sulfate and the solvent was evaporated to give a yellow oil. The resulting oil was chromatographed on silica gel using hexanes and ethyl acetate (1:1) to give ethyl 2-bromo-2(3-pyridyl)acetate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091230B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-38a9717950d0440ea0c81b2cb1362db2
출처 메모uspto-grants-2006_08