Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ethyl 3-(tributylsilyloxy)picolinate → 2-(4-Fluorobenzoyl)-3-(tributylsilyloxy)pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ethyl 3-(tributylsilyloxy)picolinate | HCID 22987980 | — |
| 반응물 | HCID 178505844 | HCID 178505844 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 2-(4-Fluorobenzoyl)-3-(tributylsilyloxy)pyridine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06479507B2 |
| 출처 데이터셋 | uspto-grants-2002_11 |
| ORD ID | ord-d3bfc719a4e94de09ad93efc2a8b4959 |
| 출처 메모 | uspto-grants-2002_11 |