Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Hydroxybenzaldehyde → 3-(2-Bromoethoxy)benzaldehyde
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Hydroxybenzaldehyde | HCID 101 | — |
| 반응물 | Acetonitrile | HCID 6342 | — |
| 반응물 | 1,1-Dibromoethane | HCID 11201 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 용매 | Diethyl Ether | HCID 3283 | — |
| 생성물 | 3-(2-Bromoethoxy)benzaldehyde | HCID 2735565 | — |
반응 단계
A mixture of 3-hydroxybenzaldehyde (5.17 g, 42.33 mmol), K2CO3 (58.5 g) and CH3CN (100 ml) was stirred at room temperature for 15 minutes, then dibromoethane (18.3 ml) was added. The reaction mixture was stirred at room temperature for 30 minutes, then at reflux for 3-4 hours. Additional dibromoethane was added and then the reaction mixture was refluxed overnight. The reaction mixture was cooled, filtered, and the filtrate was stripped to afford an oil. The oil was dissolved in ether (300 ml), washed with 5N NaOH (2×75 ml) and the ether layer was dried over MgSO4 and stripped. The residue was purified by column chromatography on silica gel eluting with 10% ethyl acetate/hexane to afford 5.23 g of 3-(2-bromoethoxy)benzaldehyde.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05958929 |
| 출처 데이터셋 | uspto-grants-1999_09 |
| ORD ID | ord-906f685a24c447c887bf4cd3a385dd1f |
| 출처 메모 | uspto-grants-1999_09 |