Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Phenylprop-2-Enal → alpha-Bromocinnamaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Phenylprop-2-Enal | HCID 307 | — |
| 반응물 | Water | HCID 962 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Bromine | HCID 24408 | — |
| 용매 | Acetic Acid | HCID 176 | — |
| 생성물 | alpha-Bromocinnamaldehyde | HCID 21585 | — |
반응 단계
1.33 g (10 mmol) cinnamaldehyde was dissolved in 5 mL glacial acetic acid and cooled on an ice-water bath. 1.62 g bromine was added, and anhydrous K2CO3 was then added, and it was stirred until no gas was evolving. After refluxing for 30 min, the reaction mixture was poured into 100 mL cold water with stirring, extracted with 50 mL ethyl ether three times. The combined ethyl ether layers were washed with water one time, saturated aqueous NaCl solution one time, dried over MgSO4 for 2 hours, filtrated, and the filtrate was dried under vacuum, and washed with anhydrous ethyl ether: petroleum ether (1:1) to give the title compound as light yellow powder.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08053577B2 |
| 출처 데이터셋 | uspto-grants-2011_11 |
| ORD ID | ord-33127781f18340369da56dfe4b8793c5 |
| 출처 메모 | uspto-grants-2011_11 |