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Ethanol → 5-Ethoxy-2-nitro-4-(trifluoromethyl)aniline

HRID 418143
ノート
印刷プレビュー

反応式

HRID 418143 の反応式
[CH3:1][CH2:2][OH:3].[K].Cl[C:6]1[C:7]([C:16]([F:19])([F:18])[F:17])=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[C:10]([NH2:12])[CH:11]=1>O>[CH2:2]([O:3][C:6]1[C:7]([C:16]([F:17])([F:19])[F:18])=[CH:8][C:9]([N+:13]([O-:15])=[O:14])=[C:10]([NH2:12])[CH:11]=1)[CH3:1]
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 702EthanolHCID 27738135-Chloro-2-nitro-4-(trifluoromethyl)anilineHCID 5462222Potassium2 回

生成物 1

HCID 223171555-Ethoxy-2-nitro-4-(trifluoromethyl)aniline収率 96%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To EtOH (500 mL) was added potassium metal (ca. 21 g, ca. 537 mmol) and the vigorous reaction had to be cooled with an ice bath. Stirring was continued until all potassium metal was dissolved. Solid commercially available 5-chloro-2-nitro-4-trifluoromethyl-phenylamine [CAS-No. 35375-74-7] (57.74 g, 240 mmol) was added in one portion and the resulting dark red mixture was stirred at 55-60° C. for 4 days. The warm reaction mixture was slowly poured into H2O (ca. 2000 mL), adjusted pH with conc. HC1 to pH 2, the yellow precipitate was filtered off, washed with H2O and dried in air at 60° C. to give a yellow solid (57.81 g, 96%), which was used without further purification. MS (ISN) 249 [M−H].

後処理

  1. customthe vigorous reaction
  2. temperatureto be cooled with an ice bath
  3. dissolutionwas dissolved
  4. stirringthe resulting dark red mixture was stirred at 55-60° C. for 4 days
  5. customThe warm reaction mixture
  6. filtrationto pH 2, the yellow precipitate was filtered off
  7. washwashed with H2O
  8. customdried in air at 60° C.

出典と根拠

ORDレコード
ord-1ce9944de14e496a852d5953a5f641f3
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093263B2

反応ノート

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