반응식
[CH:1]1[C:14]2[C:5](=[CH:6][C:7]3[C:12]([C:13]=2[C:15]([OH:17])=O)=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:20])=O>>[CH:1]1[C:14]2[C:5](=[CH:6][C:7]3[C:12]([C:13]=2[C:15]([Cl:20])=[O:17])=[CH:11][CH:10]=[CH:9][CH:8]=3)[CH:4]=[CH:3][CH:2]=1참가 물질
3
실험 절차
The 2-methyl-3,5-dihydro-5,9b-o-benzenobenz[e]isoindol-1-(2H)-one starting material was prepared as follows: a mixture of 25 g of 9-anthroic acid and 75 ml of thionyl chloride is heated under reflux for 1 hour. The excess thionyl chloride is removed under vacuum (30 mm; 90° bath temperature); 50 ml of toluene is added and the mixture is concentrated again. This operation is repeated once more to give 28.3 g of 9-anthroyl chloride as a very moisture-sensitive, yellow solid.
후처리
- temperatureis heated
- temperatureunder reflux for 1 hour
- customThe excess thionyl chloride is removed under vacuum (30 mm; 90° bath temperature)
- addition50 ml of toluene is added
- concentrationthe mixture is concentrated again
출처 및 근거
- ORD 기록
- ord-11d7fb76ca0241699d76ef7ca8b02dc5
- 출처 데이터셋
- uspto-grants-1978_05
- 특허 번호
- US04088772
연결된 노트
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