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Ethanol → N-(6-chloro-2-methoxypyridin-3-yl)formamide

HRID 546742
ノート
印刷プレビュー

反応式

HRID 546742 の反応式
[Cl-].[NH4+].[Cl:3][C:4]1[N:9]=[C:8]([O:10][CH3:11])[C:7]([N+:12]([O-])=O)=[CH:6][CH:5]=1.[CH2:15]([OH:17])C>O.[Fe]>[Cl:3][C:4]1[N:9]=[C:8]([O:10][CH3:11])[C:7]([NH:12][CH:15]=[O:17])=[CH:6][CH:5]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 107977036-Chloro-2-methoxy-3-nitropyridine

生成物 1

HCID 86628511N-(6-chloro-2-methoxypyridin-3-yl)formamide

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 962Water溶媒

反応条件

温度
85 °C

実験手順

Iron (11.9 g) and ammonium chloride (22.7 g) were added to a solution of 6-chloro-2-methoxy-3-nitropyridine (10.0 g, CAS: 40851-91-0) in ethanol (130 mL) and water (52 mL). The reaction solution was stirred at 80 to 90° C. for one hour and 20 minutes and then left to cool to room temperature. The reaction solution was filtered through celite and washed with ethanol. Then, the filtrate was concentrated under reduced pressure. The residue was diluted with ethyl acetate and water, and the organic layer was separated. The resulting organic layer was washed with brine, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The residue was diluted with THF (26 mL). The THF solution was added dropwise to a mixed solution of formic acid (20.1 mL) and acetic anhydride (20.1 mL) at room temperature. Then, the reaction solution was stirred for one hour. Ice water (120 mL) was added to the reaction solution, and the precipitated crystals were collected by filtration. The crystals were washed with water and then air-dried to obtain 5.85 g of the title compound. The property value of the compound is as follows.

後処理

  1. waitleft
  2. temperatureto cool to room temperature
  3. filtrationThe reaction solution was filtered through celite
  4. washwashed with ethanol
  5. concentrationThen, the filtrate was concentrated under reduced pressure
  6. additionThe residue was diluted with ethyl acetate and water
  7. customthe organic layer was separated
  8. washThe resulting organic layer was washed with brine
  9. dry with materialdried over anhydrous magnesium sulfate
  10. concentrationconcentrated under reduced pressure
  11. additionThe residue was diluted with THF (26 mL)
  12. additionThe THF solution was added dropwise to a mixed solution of formic acid (20.1 mL) and acetic anhydride (20.1 mL) at room temperature
  13. stirringThen, the reaction solution was stirred for one hour
  14. additionIce water (120 mL) was added to the reaction solution
  15. filtrationthe precipitated crystals were collected by filtration
  16. washThe crystals were washed with water
  17. customair-dried

出典と根拠

ORDレコード
ord-95c81ef0cc344068a6384be254aee93b
出典データセット
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07935815B2

反応ノート

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