Thionyl Chloride → 2-Chloro-5-(chloromethyl)-3-methoxypyridine
反応式
[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]=1参加物
4
実験手順
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.
後処理
- customthe reaction was quenched with saturated aqueous NaHCO3
- extractionextracted with dichloromethane (3×)
- dry with materialThe combined organic layer were dried over MgSO4
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-188665bf791d4779bc8545ca2bd1f113
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07709649B2
反応ノート
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