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 | 83% |
반응 단계
8-Hydroxyquinoline-2-carbaldehyde (5.00 g, 28.9 mmol) and imidazole (4.32 g, 63.5 mmol) were dissolved in DCM (50 mL) under N2. The reaction mixture was cooled to 0° C. after which time tert-butylchlorodimethylsilane (4.94 g, 31.8 mmol) was added. After stirring for 16 hours at ambient temperature, the reaction mixture was partitioned between DCM and H2O. The organic layer was washed with H2O and aqueous saturated NaHCO3, dried over Na2SO4, filtered and concentrated under reduced pressure to afford an orange oil. The residue was purified via flash column chromatography (10:1 Hexane/EtOAc) to provide 6.85 g (83%) of desired product as a yellow/orange oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08895550B2 |
| 출처 데이터셋 | uspto-grants-2014_11 |
| ORD ID | ord-8b72e96bd29f41a38b067d733efbf1ca |
| 출처 메모 | uspto-grants-2014_11 |