反応 #1379883

ord-8aa1143c18124e82a60df5635239728c

反応方程式

CNCCO
2-methylaminoethanol
COc1ccc([N+](=O)[O-])c(Cl)n1
2-chloro-3-nitro-6-methoxypyridine
C1COCCO1
dioxane
COc1ccc([N+](=O)[O-])c(CNCCO)n1
yellow powder
収率 70.0%
COc1ccc([N+](=O)[O-])c(CNCCO)n1
2-[(6-methoxy-3-nitro-2-pyridyl)methylamino]ethanol
収率 70.0%

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度The mixture is refluxed for 2 hours
  2. 2
    workup.STIRRINGwith stirring
  3. 3
    その他The precipitate formed
  4. 4
    ろ過is filtered off by suction
  5. 5
    その他dried under vacuum to constant weight

実験手順

1.9 g (0.01 mol) of the product 2-chloro-3-nitro-6-methoxypyridine, 30 ml of dioxane, 5 ml of water and 1.6 ml (0.02 mol) of 2-methylaminoethanol are placed in a fully equipped round-bottomed flask. The mixture is refluxed for 2 hours with stirring and is then poured onto an ice/water mixture with stirring. The precipitate formed is filtered off by suction and dried under vacuum to constant weight. 1.6 g of yellow powder are obtained, ie a yield of 70%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07238211B2uspto-grants-2007_07