Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-bromobutanimide → Ethyl 5-bromo-2-methylthiazole-4-carboxylate
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | Ethyl 2-methyl-1,3-thiazole-4-carboxylate | HCID 293353 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | Ethyl 5-bromo-2-methylthiazole-4-carboxylate | HCID 59291239 | 40.1% |
반응 단계
To a solution of ethyl 2-methyl-1,3-thiazole-4-carboxylate (14.53 g) in MeCN (150 mL) was added NBS (22.66 g), followed by heating under reflux for 3 hours. To the reaction mixture was added NBS (7.55 g), followed by heating under reflux for 2 hours. Under ice-cooling, to the reaction mixture was added a saturated aqueous NaHCO3 solution, followed by stirring for 5 minutes, and then extraction with EtOAc. The organic layer was dried over MgSO4 and then concentrated under reduced pressure. The residue obtained was purified by silica gel column chromatography (hexane:EtOAc=from 100:0 to 60:40) to obtain ethyl 5-bromo-2-methyl-1,3-thiazole-4-carboxylate (8.52 g) as a yellow solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08367696B2 |
| 출처 데이터셋 | uspto-grants-2013_02 |
| ORD ID | ord-a8c009059a5f495dae254bba06320339 |
| 출처 메모 | uspto-grants-2013_02 |