Chloroform → 3,6-Dichloro-2-(dichloromethyl)pyridine
반응식
Cl[C:2]1[C:7]([Cl:8])=[CH:6][CH:5]=[C:4]([Cl:9])[N:3]=1.[CH:10](Cl)([Cl:12])[Cl:11].[OH-].[Na+]>CN1CCCC1=O>[Cl:8][C:7]1[C:2]([CH:10]([Cl:12])[Cl:11])=[N:3][C:4]([Cl:9])=[CH:5][CH:6]=1참가 물질
5
실험 절차
2,3,6-Trichloropyridine (1.0 g, 0.0055 mole) was combined with 4 g N-methylpyrrolidone, 4 g (0.033 mole) of chloroform, and 1.0 g of 50 percent aqueous sodium hydroxide (0.013 mole). The resulting mixture was stirred and warmed mildly for about 1 hour at which time the product was found to be present in the reaction mixture by gas chromatography and mass spectrometry using an authentic sample of the product as a standard. After standing overnight at ambient temperature the title compound represented about 1.7 percent of the pyridines in the mixture.
후처리
- temperaturewarmed mildly for about 1 hour at which time the product
출처 및 근거
- ORD 기록
- ord-cf5615007f874751a6cc3524fcd7feb8
- 출처 데이터셋
- uspto-grants-1988_04
- 특허 번호
- US04739070
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