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[C:1](OC(=O)C)(=O)C.C(O)=O.[F:11][C:12]1[CH:17]=[CH:16][C:15]([C:18](=[O:24])[CH2:19][S:20]([CH3:23])(=[O:22])=[O:21])=[C:14]([NH:25][CH3:26])[CH:13]=1.[OH2:27]>ClC(Cl)Cl>[F:11][C:12]1[CH:17]=[CH:16][C:15]([C:18](=[O:24])[CH2:19][S:20]([CH3:23])(=[O:22])=[O:21])=[C:14]([CH:13]=1)[N:25]([CH3:1])[CH:26]=[O:27]참가 물질
실험 절차
A mixture of acetic anhydride (19.8 ml) and formic acid (13.5 ml) was stirred and heated at 60° under nitrogen for 2 hours. 1-(4-Fluoro-2-methylaminophenyl)-2-methylsulphonylethanone (10.0 g), was added portionwise to the mixture at ambient temperature with stirring. The mixture was stirred at 30° for 30 minutes. Water (30 ml) was added to the reaction mixture which was then stirred at 30° for 30 minutes. Concentration of the reaction mixture by evaporation in vacuo gave a green oil. The oil was dissolved in trichloromethane (50 ml) and washed with aqueous sodium hydrogen carbonate solution (7% w/w; 2×30 ml). The trichloromethane extract was dried (magnesium sulphate) and evaporated in vacuo to give a green oil which solidified at ambient temperature. Recrystallisation from toluene gave 5'-fluoro-N-methyl-2'-methylsulphonylacetylformanilide, m.p. 94.5°-95.5°.
후처리
- temperatureheated at 60° under nitrogen for 2 hours
- stirringwith stirring
- stirringThe mixture was stirred at 30° for 30 minutes
- stirringwas then stirred at 30° for 30 minutes
- customConcentration of the reaction mixture by evaporation in vacuo
- customgave a green oil
- washwashed with aqueous sodium hydrogen carbonate solution (7% w/w; 2×30 ml)
- extractionThe trichloromethane extract
- dry with materialwas dried (magnesium sulphate)
- customevaporated in vacuo
- customto give a green oil which
- customsolidified at ambient temperature
- customRecrystallisation from toluene
출처 및 근거
- ORD 기록
- ord-40e826fdf0a0493684ab04e6140c33c8
- 출처 데이터셋
- uspto-grants-1991_04
- 특허 번호
- US05011931
연결된 노트
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