Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
N-bromobutanimide → (5-bromo-1-methyl-1H-imidazol-2-yl)methanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | N-bromobutanimide | HCID 67184 | — |
| 반응물 | (1-methyl-1H-imidazol-2-yl)methanol | HCID 573612 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (5-bromo-1-methyl-1H-imidazol-2-yl)methanol | HCID 23445171 | 67% |
반응 단계
1-Methylimidazole-2-methanol (3.15 g, 28 mmol) (R. J. Sundberg; P. V. Nguyen; Med. Chem. Res. 7, 2, 1997, 123-136) was suspensed in THF (75 ml) at −20° C. and treated slowly (within 30 min) with N-bromosuccinimide (4.9 g, 27 mmol). The reaction mixture was allowed to warm up slowly to room temperature and quenched with saturated aqueous NaHCO3 solution (50 ml). The aqueous layer was extracted 3 times with AcOEt. The combined extracts were washed with saturated aqueous NaHCO3 solution, dried over Na2SO4, filtered and the solvent was removed in vacuo. The residue was chromatographed (silica, elution first with AcOEt/hexane 1:1, then with CH2Cl2/MeOH 95:05) to provide the title compound (2.11 g, 67%) as a white solid. MS: m/e=191.2 (M+).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06610723B2 |
| 출처 데이터셋 | uspto-grants-2003_08 |
| ORD ID | ord-8ad3e346f50746bc81bc84d5ea1bcb29 |
| 출처 메모 | uspto-grants-2003_08 |