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Water → 3-Fluoro-2-hydrazinyl-5-(trifluoromethyl)pyridine

HRID 1748555
ノート
印刷プレビュー

反応式

HRID 1748555 の反応式
O.[NH2:2][NH2:3].F[C:5]1[C:10]([F:11])=[CH:9][C:8]([C:12]([F:15])([F:14])[F:13])=[CH:7][N:6]=1.O>C(O)C>[F:11][C:10]1[C:5]([NH:2][NH2:3])=[N:6][CH:7]=[C:8]([C:12]([F:15])([F:14])[F:13])[CH:9]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 24654Hydrazine hydrate (1:1)HCID 134215472,3-Difluoro-5-(trifluoromethyl)pyridine

生成物 1

HCID 552813773-Fluoro-2-hydrazinyl-5-(trifluoromethyl)pyridine

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒2 回

実験手順

To a solution of hydrazine hydrate (100%) (3.45 ml) in ethanol (150 ml) was added dropwise a solution of 2,3-difluoro-5-(trifluoromethyl)pyridine (4.45 g) in ethanol (50 ml) at room temperature, stirred at the same temperature for 2 hours, and then additionally stirred at 80° C. for 2 hours. Then, the mixture was allowed to cool, water was added thereto, and the organic solvent was evaporated in vacuo. The precipitated solid was collected by filtration, and washed with water to give 3-fluoro-5-(trifluoromethyl)pyridin-2-ylhydrazine as a white solid.

後処理

  1. stirringadditionally stirred at 80° C. for 2 hours
  2. temperatureto cool
  3. customthe organic solvent was evaporated in vacuo
  4. filtrationThe precipitated solid was collected by filtration
  5. washwashed with water

出典と根拠

ORDレコード
ord-dbc2f79b9a6c4bc5931dbe069eb53496
出典データセット
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09150555B2

反応ノート

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