Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tetrahydrofuran → 2-Chloro-5-methoxypyridine-3-boronic acid
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tetrahydrofuran | HCID 8028 | — |
| 반응물 | Hexane | HCID 8058 | — |
| 반응물 | Triisopropyl borate | HCID 21531 | — |
| 반응물 | 3-Bromo-2-chloro-5-methoxypyridine | HCID 46738814 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 생성물 | 2-Chloro-5-methoxypyridine-3-boronic acid | HCID 46738816 | 71% |
반응 단계
2.5 M n-BuLi in hexane (3.7 mL, 9.3 mmol) was added slowly to a stirred premixed solution of 3-bromo-2-chloro-5-methoxypyridine (1.73 g, 7.8 mmol) and triisopropyl borate (2.1 mL, 9.3 mmol) in THF (10.0 mL, 122 mmol) at −78° C., and the resulting deep colored mixture was stirred at the same temperature for 1 h and then allowed to warm up to room temperature over 1 h. The reaction was quenched with 1 N NaOH(aq) and then some EtOAc. The separated aqueous layer was acidified with 5N HCl until pH about 5 and then extracted with EtOAc(×2) and the combined organic layers were washed with brine, dried over Na2SO4, and concentrated to give 2-chloro-5-methoxypyridin-3-ylboronic acid (1.0276 g, 71%) as a brown solid. LCMS (API-ES) m/z 188 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08772480B2 |
| 출처 데이터셋 | uspto-grants-2014_07 |
| ORD ID | ord-256e3b84f8bc4fdcb672bff1fa63a78a |
| 출처 메모 | uspto-grants-2014_07 |