Thionyl Chloride → 2-Chloro-5-(chloromethyl)-3-methoxypyridine
반응식
[Cl:1][C:2]1[N:7]=[CH:6][C:5]([CH2:8]O)=[CH:4][C:3]=1[O:10][CH3:11].S(Cl)([Cl:14])=O>ClCCl>[Cl:1][C:2]1[C:3]([O:10][CH3:11])=[CH:4][C:5]([CH2:8][Cl:14])=[CH:6][N:7]=1참가 물질
4
실험 절차
To a solution of (6-chloro-5-methoxypyridin-3-yl)methanol (0.50 g, 2.9 mmol) in dichloromethane (14 mL) at 25° C. was added thionyl chloride (230 μL, 3.2 mmol) dropwise. Let stir for 5 h, then the reaction was quenched with saturated aqueous NaHCO3 and extracted with dichloromethane (3×). The combined organic layer were dried over MgSO4 and concentrated to furnish the product 2-chloro-5-chloromethyl-3-methoxypyridine that was 96% pure by GC-MS. The product was used immediately in the next step without further purification. GC-MS: Exact mass calcd for C7H7Cl2NO [M]+, 191. Found 191.
후처리
- customthe reaction was quenched with saturated aqueous NaHCO3
- extractionextracted with dichloromethane (3×)
- dry with materialThe combined organic layer were dried over MgSO4
- concentrationconcentrated
출처 및 근거
- ORD 기록
- ord-8747e36d5caa4ad88cc853932e162e7b
- 출처 데이터셋
- uspto-grants-2012_05
- 특허 번호
- US08178565B2
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