Thionyl Chloride → N-(3',4'-Dichlorophenyl)-3,4-dimethyl-2-chloro-5-oxo-2,5-dihydropyrrole
반응식
[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13](=[O:14])[C:12]([CH3:15])=[C:11]([CH3:16])[CH:10]2O)[CH:5]=[CH:6][C:7]=1[Cl:8].S(Cl)([Cl:20])=O>>[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[C:13](=[O:14])[C:12]([CH3:15])=[C:11]([CH3:16])[CH:10]2[Cl:20])[CH:5]=[CH:6][C:7]=1[Cl:8]참가 물질
3
실험 절차
27.2 g of N-(3',4'-dichlorophenyl)-3,4-dimethyl-2-hydroxy-5-oxo-2,5-dihydropyrrole (see Example 3) is added to 25 ml of thionyl chloride, with an intense evolution of gas occurring. After being stirred for one hour at 50°, the mixture is concentrated by evaporation in vacuo. The solid residue is triturated with petroleum ether to obtain 27.4 g (95% of theory) of the above compound in the form of light-yellow crystals, m.p. 95°-96°.
후처리
- concentrationthe mixture is concentrated by evaporation in vacuo
- customThe solid residue is triturated with petroleum ether
- customto obtain 27.4 g (95% of theory) of the above compound in the form of light-yellow crystals, m.p. 95°-96°
출처 및 근거
- ORD 기록
- ord-911ca978e7994602922686e1b9d8dd0d
- 출처 데이터셋
- uspto-grants-1980_09
- 특허 번호
- US04220655
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