Lithium Hydroxide → 6-Bromo-3-hydroxypyridine-2-carboxylic acid
反応式
[Br:1][C:2]1[N:7]=[C:6]([C:8]([O:10]C)=[O:9])[C:5]([OH:12])=[CH:4][CH:3]=1.[Li+].[OH-]>CO>[Br:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=[O:9])[C:5]([OH:12])=[CH:4][CH:3]=1参加物
4
実験手順
Methyl 6-bromo-3-hydroxypicolinate (26B) (464 mg, 2 mmol) in MeOH (0.5 mL) was added to a solution of LiOH (200 mg in 2 mL water). The reaction mixture was stirred at rt for 2 h. The product precipitated out of solution and was filtered, washed with water, and dried under reduced pressure to provide the desired product 6-bromo-3-hydroxypicolinic acid (55A). 1H NMR (300 MHz, CDCl3): 7.6 (1H, d), 7.32 (1H, d).
後処理
- customThe product precipitated out of solution
- filtrationwas filtered
- washwashed with water
- customdried under reduced pressure
出典と根拠
- ORDレコード
- ord-9bd013136bfd40f29f42030ad12d2074
- 出典データセット
- uspto-grants-2012_02
- 特許番号
- US08114893B2
反応ノート
読み込み中…