Acetic Acid → 3-(2,2-Dichlorovinyloxy)-benzaldehyde
반응식
[Cl:1][C:2]([Cl:13])=[CH:3][O:4][C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH2:8]Br.C1N2CN3CN(C2)CN1C3.C(O)(=[O:26])C.Cl>C(Cl)(Cl)(Cl)Cl.O>[Cl:1][C:2]([Cl:13])=[CH:3][O:4][C:5]1[CH:6]=[C:7]([CH:10]=[CH:11][CH:12]=1)[CH:8]=[O:26]참가 물질
실험 절차
3(2,2-Dichlorovinyloxy)benzyl bromide (2.5 g) was carefully added to a stirred solution of hexamethylene tetramine (2.1 g) in carbon tetrachloride (20 ml) at the ambient temperature. After 5 minutes the precipitate was collected by filtration and washed with acetone. The solid thus obtained was added to aqueous acetic acid solution (50% by weight, 16 ml) and the mixture refluxed for 1 hour. A mixture of water (16 ml) and concentrated hydrochloric acid (4.5 ml) was then added and the mixture refluxed for a further 15 minutes. After cooling the mixture was extracted with chloroform, the extracts washed with water (twice), dried over anhydrous magnesium sulphate and the solvent removed by evaporation under reduced pressure to yield a residue of substantially pure 3(2,2-dichlorovinyloxy)benzaldehyde, identification of which was confirmed by infra-red and nuclear magnetic resonance spectroscopy.
후처리
- filtrationAfter 5 minutes the precipitate was collected by filtration
- washwashed with acetone
- customThe solid thus obtained
- temperaturethe mixture refluxed for 1 hour
- additionwas then added
- temperaturethe mixture refluxed for a further 15 minutes
- temperatureAfter cooling the mixture
- extractionwas extracted with chloroform
- washthe extracts washed with water (twice),
- dry with materialdried over anhydrous magnesium sulphate
- customthe solvent removed by evaporation under reduced pressure
출처 및 근거
- ORD 기록
- ord-60b47de767b94bd1aaf9299415ceccb5
- 출처 데이터셋
- uspto-grants-1978_05
- 특허 번호
- US04091110
반응 노트
불러오는 중…