反応式
N[C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([Br:9])=[CH:4][N:3]=1.[BrH:10].BrBr.N([O-])=O.[Na+].[OH-].[Na+]>O.CCOCC.CCCCCC>[Br:10][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([Br:9])=[CH:4][N:3]=1参加物
反応条件
- 温度
- 2 °C
実験手順
2-Amino-5-bromo-4-methylpyridine (2.0 g, 10.7 mmol) was dissolved in 48% aqueous HBr (14 mL, 123 mmol) and cooled to 2° C. in a salt/ice bath. Bromine (1.65 mL, 32.1 mmol) was added dropwise keeping the internal temperature below 2° C. A solution of sodium nitrite (3.69 g, 53.5 mmol) in water (5 mL) was added keeping the internal temperature below 5° C. and stirred for 1 h between 0° C. and 5° C. The pH was adjusted to ˜13 by slow addition with cooling of 50% NaOH (aq). After warming to r.t. the reaction was extracted with ether, the organics were dried over MgSO4 and concentrated to give a brown oil. Flash chromatography on silica gel eluting with 5% ether/hexane gave the product as a white solid (1.83 g, 7.29 mmol, 68%). MS [M+H]+: 251.9; tR=2.3 min. (method 1)
後処理
- customthe internal temperature below 2° C
- customthe internal temperature below 5° C.
- additionThe pH was adjusted to ˜13 by slow addition
- temperatureAfter warming to r.t. the reaction
- extractionwas extracted with ether
- dry with materialthe organics were dried over MgSO4
- concentrationconcentrated
- customto give a brown oil
出典と根拠
- ORDレコード
- ord-806cdb0b57b24cd9bd2eb8f8db7d2ead
- 出典データセット
- uspto-grants-2011_12
- 特許番号
- US08084614B2
関連ノート
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