Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Ammonium Hydroxide → 7-Methoxy-2,6-dimethylquinoline
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | 3-Methoxy-4-methylaniline | HCID 27882 | — |
| 반응물 | Crotonaldehyde | HCID 447466 | — |
| 용매 | Hydrochloric Acid | HCID 313 | — |
| 생성물 | 7-Methoxy-2,6-dimethylquinoline | HCID 86707471 | 42.5% |
반응 단계
To 3-methoxy-4-methylaniline (1.0 g, 7.29 mmol) in refluxing in 6N HCl (50 mL) was added dropwise (E)-but-2-enal (1.02 g, 14.6 mmol). The reaction was heated to reflux for 2 hours then cooled down and neutralized with NH4OH. The organic phase was extracted with DCM and the combined organic phases dried over MgSO4, filtered and concentrated under reduced pressure to leave a dark residue. The residue was purified by reverse phase chromatography (SP4, 25M, eluting with a gradient of water/ACN 100:0 to 0:100, 20 column volumes) to yield 7-methoxy-2,6-dimethylquinoline (580 mg, 29.7% yield) as a beige solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08889704B2 |
| 출처 데이터셋 | uspto-grants-2014_11 |
| ORD ID | ord-d1a62e775ff14853b31c0c1618bab9fe |
| 출처 메모 | uspto-grants-2014_11 |