Benzoyl Peroxide → 3-Formyl-2-(4-methoxy-benzenesulfonylamino)-benzoic acid methyl ester
반응식
[CH3:1][O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH3:10])[C:5]=1[NH:11][S:12]([C:15]1[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][CH:16]=1)(=[O:14])=[O:13].C(OOC(=O)C1C=CC=CC=1)(=[O:31])C1C=CC=CC=1.BrN1C(=O)CCC1=O>C(Cl)(Cl)(Cl)Cl>[CH3:1][O:2][C:3](=[O:23])[C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([CH:10]=[O:31])[C:5]=1[NH:11][S:12]([C:15]1[CH:16]=[CH:17][C:18]([O:21][CH3:22])=[CH:19][CH:20]=1)(=[O:14])=[O:13]참가 물질
실험 절차
To a solution of 1.0 g (2.985 mmol) of the product of Example 3 in 100 mL of carbon tetrachloride was added 0.20 g of dibenzoyl peroxide and 1.168 g (6.568 mmol) of N-bromosuccinimide. The resulting mixture was refluxed for 18 h, cooled, washed with sodium bisulfite solution and water, dried over MgSO4, filtered and concentrated in vacuo. The residue was diluted with 10 mL of THF and 10 mL of 1N sodium hydroxide solution and the mixture was stirred at room temperature for 3 h. The reaction mixture was then acidified with 5% HCl and extracted with ether. The organics were dried over MgSO4, filtered and concentrated in vacuo. The residue was triturated with ether to provide 0.477 g (47%) of the product as a white solid. Electrospray Mass Spec: 350.1 (M+H)+.
후처리
- temperatureThe resulting mixture was refluxed for 18 h
- temperaturecooled
- washwashed with sodium bisulfite solution and water
- dry with materialdried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- additionThe residue was diluted with 10 mL of THF and 10 mL of 1N sodium hydroxide solution
- extractionextracted with ether
- dry with materialThe organics were dried over MgSO4
- filtrationfiltered
- concentrationconcentrated in vacuo
- customThe residue was triturated with ether
출처 및 근거
- ORD 기록
- ord-e18fa2d324a4447ea53ad42d909ff013
- 출처 데이터셋
- uspto-grants-1999_07
- 특허 번호
- US05929097
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