Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → 7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-one
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 1-Bromo-4-chlorobutane | HCID 81364 | — |
| 반응물 | 7-Hydroxy-3,4-dihydrocarbostyril | HCID 2785758 | — |
| 용매 | Hexane | HCID 8058 | — |
| 생성물 | 7-(4-Chlorobutoxy)-1,2,3,4-tetrahydroquinolin-2-one | HCID 10467467 | 78% |
반응 단계
1-bromo-4-chloro-butane (3.4 g, 20 mmol), anhydrous potassium carbonate powder (4.14 g, 30 mmol) and 7-hydroxy-3,4-dihydro-2(1H)-quinolinone (1.63 g, 10 mmol) are added to 10 ml of acetone and reflux for 24 hours. The reaction solution is evaporated to dryness and dispersed with 20 ml of dichloromethane and 20 ml of water respectively. The organic layer is extracted with water (20 ml×2) and saturated saline (20 ml) successively, dried over anhydrous magnesium sulfate, and evaporated to dryness to obtain a light yellow powder. The powder is slurried with n-hexane (20 ml×3), filtered, and dried to obtain 1.98 g of 7-(4-chlorobutoxy)-3,4-dihydro-2(1H)-quinolinone, with a yield of 78%.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08653069B2 |
| 출처 데이터셋 | uspto-grants-2014_02 |
| ORD ID | ord-2745d54df7e648f2b375b162ee852eb9 |
| 출처 메모 | uspto-grants-2014_02 |