Ammonium Hydroxide → 5-Amino-2-(trifluoromethyl)benzonitrile

HRID 517723ノート

反応式

HRID 517723 の反応式
[OH-].[NH4+:2].F[C:4]1[CH:5]=[CH:6][C:7]([C:12]([F:15])([F:14])[F:13])=[C:8]([CH:11]=1)[C:9]#[N:10]>O1CCOCC1>[NH2:2][C:4]1[CH:5]=[CH:6][C:7]([C:12]([F:15])([F:14])[F:13])=[C:8]([CH:11]=1)[C:9]#[N:10]

参加物

4

反応物 2

HCID 14923Ammonium HydroxideHCID 27375515-Fluoro-2-(trifluoromethyl)benzonitrile

生成物 1

HCID 121049585-Amino-2-(trifluoromethyl)benzonitrile

試薬・触媒・溶媒 1

HCID 312751,4-Dioxane溶媒

実験手順

Ammonium hydroxide solution (50 mL) was added to a stirred solution of 5-fluoro-2-(trifluoromethyl)benzonitrile (commercially available, for example from Alfa Aesar, Ward Hill, Mass., USA, 2.0 g, 10.6 mmol) in 1,4-dioxane (10 mL) and the reaction mixture was heated to 130° C. for 20 h under 200 psi pressure in a steel bomb. The reaction mixture was evaporated to dryness, and the residue was diluted with DCM and washed with water. The organic layer was dried over anhydrous Na2SO4 and concentrated under reduced pressure to afford the crude product. This was purified by column chromatography (100-200 mesh silica gel), eluting with 20%-40% EtOAc/petroleum ether, to give the title compound (1.2 g).

後処理

  1. customThe reaction mixture was evaporated to dryness
  2. additionthe residue was diluted with DCM
  3. washwashed with water
  4. dry with materialThe organic layer was dried over anhydrous Na2SO4
  5. concentrationconcentrated under reduced pressure
  6. customto afford the crude product
  7. customThis was purified by column chromatography (100-200 mesh silica gel)
  8. washeluting with 20%-40% EtOAc/petroleum ether

出典と根拠

ORDレコード
ord-380356f670df4645a44956b9e8e5707e
出典データセット
uspto-grants-2015_08
特許番号
US09115132B2

反応ノート

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