Thionyl Chloride → HCID 22938786, 화합물
반응식
[CH2:1]([N:3]1[CH:7]=[N:6][N:5]=[C:4]1[CH2:8]O)[CH3:2].S(Cl)([Cl:12])=O>>[ClH:12].[Cl:12][CH2:8][C:4]1[N:3]([CH2:1][CH3:2])[CH:7]=[N:6][N:5]=1참가 물질
3
실험 절차
To 4-ethyl-3-hydroxymethyl-4H-1,2,4-triazole (4.6 g), thionyl chloride (36 ml) was slowly added at 0° C. The mixture was heated to reflux for 1 hour, and concentrated under reduced pressure. To the residue was added ethyl acetate and ethanol, and the precipitated crystals were collected by filtration. The crystals were washed with ethyl acetate, to give 3-chloromethyl-4-ethyl-4H-1,2,4-triazole hydrochloride (4.22 g) as orange crystals.
후처리
- temperatureThe mixture was heated
- temperatureto reflux for 1 hour
- concentrationconcentrated under reduced pressure
- additionTo the residue was added ethyl acetate and ethanol
- filtrationthe precipitated crystals were collected by filtration
- washThe crystals were washed with ethyl acetate
출처 및 근거
- ORD 기록
- ord-72fe571441664a4e9be409866d900805
- 출처 데이터셋
- uspto-grants-2007_08
- 특허 번호
- US07262185B2
반응 노트
불러오는 중…