ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Ethanol → 2-Amino-2-methyl-4-(2-trifluoromethylphenyl)butyronitrile

HRID 9929
ノート
印刷プレビュー

反応式

HRID 9929 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[CH2:9][CH2:10]C(=O)C.[C-:16]#[N:17].[Na+].[Cl-].[NH4+:20].[CH2:21](O)[CH3:22]>N>[NH2:20][C:21]([CH3:22])([CH2:10][CH2:9][C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][C:3]=1[C:2]([F:15])([F:14])[F:1])[C:16]#[N:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 702EthanolHCID 8929Sodium CyanideHCID 25517Ammonium ChlorideHCID 117460214-[2-(Trifluoromethyl)phenyl]butan-2-one

生成物 1

HCID 112187182-Amino-2-methyl-4-(2-trifluoromethylphenyl)butyronitrile

試薬・触媒・溶媒 1

HCID 222Ammonia溶媒

実験手順

1.5 g of 4-(2-trifluoromethylphenyl)butan-2-one, 0.41 g of sodium cyanide and 0.56 g of ammonium chloride are dissolved in 77 ml of a 2M solution of ammonia in ethanol and the mixture is stirred at ambient temperature for 7 h. The mixture is subsequently concentrated under reduced pressure and the residue is redissolved in ethyl acetate and washed with water and three times with saturated sodium chloride solution. The organic phase is separated, dried with magnesium sulfate and evaporated under reduced pressure. After purifying the residue by flash chromatography, the title compound is thus obtained.

後処理

  1. concentrationThe mixture is subsequently concentrated under reduced pressure
  2. dissolutionthe residue is redissolved in ethyl acetate
  3. washwashed with water and three times with saturated sodium chloride solution
  4. customThe organic phase is separated
  5. dry with materialdried with magnesium sulfate
  6. customevaporated under reduced pressure
  7. customAfter purifying the residue by flash chromatography

出典と根拠

ORDレコード
ord-f7bffe1edf2743528fa2a6dad5094133
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07091371B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート