Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Imidazole → 8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Imidazole | HCID 795 | — |
| 반응물 | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| 반응물 | 8-Hydroxy-2-quinolinecarboxaldehyde | HCID 599342 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 8-(Tert-butyldimethylsilyloxy)quinoline-2-carbaldehyde | HCID 58567082 | 95.2% |
반응 단계
To a solution of 8-hydroxyquinoline-2-carbaldehyde (15.0 g, 86.62 mmol) and imidazole (12.97 g, 190.6 mmol) in anhydrous CH2Cl2 (250 mL) at 0° C. was added tert-butylchlorodimethylsilane (14.36 g, 95.28 mmol). The mixture was allowed to warm slowly to ambient temperature over 16 hours and then partitioned between CH2Cl2 and water. The aqueous phase was extracted with CH2Cl2 and the combined organic phases were washed successively with saturated NaHCO3, water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by silica gel pad filtration eluting with hexanes followed by 19:1 ethyl acetate/hexanes to provide 23.69 g (95%) of desired product as a dark yellow oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08987251B2 |
| 출처 데이터셋 | uspto-grants-2015_03 |
| ORD ID | ord-dce37435330049cb8a94a5fc1ae3ea15 |
| 출처 메모 | uspto-grants-2015_03 |