반응식
Cl.Cl[CH2:3][C:4]1[N:5]=[CH:6][NH:7][CH:8]=1.CN(C)C=O.O.[C:15]1([CH3:23])[CH:20]=[C:19]([CH3:21])[CH:18]=[C:17]([CH3:22])[CH:16]=1>>[CH3:23][C:15]1[CH:20]=[C:19]([CH3:21])[CH:18]=[C:17]([CH3:22])[C:16]=1[CH2:3][C:4]1[N:5]=[CH:6][NH:7][CH:8]=1참가 물질
5
실험 절차
3.0 g of 4-chloromethylimidazole hydrochloride are suspended in 20 ml of mesitylene. 5 ml of dimethylformamide are added and the reaction mixture is refluxed for 12 hours, then cooled. 30 ml of water are added, the layers are separated, and the aqueous phase is washed with chloroform. The aqueous solution is then made alkaline with sodium carbonate solution and extracted with chloroform. The combined chloroform extracts are washed with water and evaporated to dryness. The residue, which is crude 4-(2',4',6'-trimethylbenzyl)imidazole, is converted to the hydrochloride by treatment with concentrated hydrochloric acid. The hydrochloride salt melts at 166°-169° C.
후처리
- temperaturethe reaction mixture is refluxed for 12 hours
- temperaturecooled
- customthe layers are separated
- washthe aqueous phase is washed with chloroform
- extractionextracted with chloroform
- washThe combined chloroform extracts are washed with water
- customevaporated to dryness
출처 및 근거
- ORD 기록
- ord-16847070d393484a890e2ce81c4eaa82
- 출처 데이터셋
- uspto-grants-1984_04
- 특허 번호
- US04443466
연결된 노트
불러오는 중…