Thionyl Chloride → 2-Chloro-4-methyl-5-nitropyridine
反応式
[CH3:1][C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][NH:5][C:4](=O)[CH:3]=1.S(Cl)([Cl:14])=O>CN(C)C=O>[Cl:14][C:4]1[CH:3]=[C:2]([CH3:1])[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][N:5]=1参加物
実験手順
A mixture of 4-methyl-5-nitro-1H-pyridine-2-one (5.00 g, 32.44 mmol), thionyl chloride (20 ml), and two drops of dimethylformamide was heated at reflux under nitrogen for 52 hours. The resultant orange colored solution was evaporated under reduced pressure, and a small amount of anhydrous toluene was added and then removed via evaporation under reduced pressure to remove traces of thionyl chloride. The residual oil then passed through a silica gel filter (dried at 150° C. under vacuum overnight, approximately 100 g) followed by methylene chloride (1 1). This filtrate was evaporated under reduced pressure to afford 2-chloro-4-methyl-5-nitropyridine (5.30 g, 30.71 mmol, 95%) as an orange oil, which crystallized below 0° C.; IR (CHCl3) 1,605, 1,550, 1,520, 1,450, 1,360, 1,345 cm-1 ; 1H NMR (CDCl3) δ 9.03 (s, 1H), 7.83 (s, 1H), 2.60 (s, 3H); LRMS (m/z, relative intensity) 174 (25), 173 (19), 172 (M+, 68), 157 (74), 155 (100), 128 (27), 101 (47), 100 (55), 99 (74), 90 (43), 75 (36).
後処理
- temperaturewas heated
- temperatureat reflux under nitrogen for 52 hours
- customThe resultant orange colored solution was evaporated under reduced pressure
- additiona small amount of anhydrous toluene was added
- customremoved via evaporation under reduced pressure
- customto remove traces of thionyl chloride
- filtrationfilter
- custom(dried at 150° C. under vacuum overnight, approximately 100 g)
- customThis filtrate was evaporated under reduced pressure
出典と根拠
- ORDレコード
- ord-5b8cef8327204f4b90a1b71cbd1bd78d
- 出典データセット
- uspto-grants-1992_12
- 特許番号
- US05169947
反応ノート
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