반응식
[C:1]1(=[O:10])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH2:3][CH2:2]1.C1C(=O)N([Br:18])C(=O)C1>C(Cl)(Cl)(Cl)Cl>[Br:18][CH:3]1[C:4]2[C:9](=[CH:8][CH:7]=[CH:6][CH:5]=2)[C:1](=[O:10])[CH2:2]1참가 물질
4
실험 절차
1-Indanone (1 g) and NBS (1.4 g) was mixed with dry CCl4 (20 ml). A catalytic amount of AlBN was added and the mixture was refluxed for 30 minutes and excited with light using 250 W lamp. The mixture was cooled in an ice bath and filtered. The filtrate was concentrated in an evaporator and used without further purification for the next step. Yield was 1.5 g.
후처리
- temperaturethe mixture was refluxed for 30 minutes
- temperatureThe mixture was cooled in an ice bath
- filtrationfiltered
- concentrationThe filtrate was concentrated in an evaporator
- customused without further purification for the next step
출처 및 근거
- ORD 기록
- ord-c54a0fd89f4a4e89ae60c4b36eb93b67
- 출처 데이터셋
- uspto-grants-2002_03
- 특허 번호
- US06362211B1
연결된 노트
불러오는 중…