돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1017667생성일: 2026년 10월 25일

Ethyl 3-(tributylsilyloxy)picolinate → 2-(4-Fluorobenzoyl)-3-(tributylsilyloxy)pyridine

https://huagongshe.com/reaction/1017667

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl 3-(tributylsilyloxy)picolinateHCID 22987980—
반응물HCID 178505844HCID 178505844—
용매TetrahydrofuranHCID 8028—
생성물2-(4-Fluorobenzoyl)-3-(tributylsilyloxy)pyridineHCID 22987964—

반응 단계

A solution of ethyl 3-(tributylsilyloxy)picolinate (19 g, 35 mmol) in tetrahydrofuran (100 ml) was cooled to 0° C. and 4-fluorophenylmagnesium chloride (52 ml, 1.0 M in tetrahydrofuran) was added dropwise. After 30 min., the reaction mixture was quenched with water and the product was extracted with ethyl acetate. The organic layer was dried over sodium sulfate and concentrated in vacuo. Purification on a silica gel column using ethyl acetate-hexane (2:98) as the eluant gave 2-(4-fluorobenzoyl)-3-(tributylsilyloxy)pyridine (3.75 g).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06479507B2
출처 데이터셋uspto-grants-2002_11
ORD IDord-d3bfc719a4e94de09ad93efc2a8b4959
출처 메모uspto-grants-2002_11