Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetic Acid → 4-(2-Acetyl-3-oxo-1-butenyl)benzonitrile
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetic Acid | HCID 176 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | Acetylacetone | HCID 31261 | — |
| 반응물 | 4-Cyanobenzaldehyde | HCID 66042 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 4-(2-Acetyl-3-oxo-1-butenyl)benzonitrile | HCID 367453 | — |
반응 단계
2.3 g (17.5 mmol) of 4-formylbenzonitrile, 1.98 ml (19.29 mmol) of 2,4-pentanedione, 1 ml (26 mmol) of acetic acid and 0.34 ml (3.5 mmol) of piperidine in 40 ml of anhydrous dichloromethane are stirred under reflux with a water trap for 24 h. After cooling, the reaction solution is washed successively with saturated sodium bicarbonate solution and saturated sodium chloride solution. The organic phase is dried over magnesium sulfate and concentrated. The residue is recrystallized from diethyl ether. 3.18 g (85% of theory) of the title compound are obtained as a pale brown solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08399471B2 |
| 출처 데이터셋 | uspto-grants-2013_03 |
| ORD ID | ord-45ed79f9ee9e4308ae54dab9054494e2 |
| 출처 메모 | uspto-grants-2013_03 |