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Sodium Dithionite → 2-{[2-Amino-6-(trifluoromethyl)phenyl]amino}ethanol

HRID 1991200
ノート
印刷プレビュー

反応式

HRID 1991200 の反応式
[N+:1]([C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:13])([F:12])[F:11])[C:5]=1[NH:14][CH2:15][CH2:16][OH:17])([O-])=O.S(S([O-])=O)([O-])=O.[Na+].[Na+]>CO.O>[NH2:1][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]([F:12])([F:13])[F:11])[C:5]=1[NH:14][CH2:15][CH2:16][OH:17]
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

5

反応物 2

HCID 24489Sodium DithioniteHCID 113571292-([2-Nitro-6-(trifluoromethyl)phenyl]amino}ethanol

生成物 1

HCID 111953562-{[2-Amino-6-(trifluoromethyl)phenyl]amino}ethanol収率 89.9%

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒2 回

反応条件

温度
60 °C

実験手順

To a solution of 2-{[2-nitro-6-(trifluoromethyl)phenyl]amino}ethanol (0.72 g, 2.88 mmol) in methanol (30 mL) a suspension of 85% sodium hydrosulfite (2.0 g, 9.8 mmol) in water (6 mL) was added. Additional water (4 mL) was added, and the mixture was heated at 60° C. for 15 min. The reaction mixture was cooled and concentrated in vacuo. The residue was extracted with ethyl acetate, and the organic phase was dried over magnesium sulfate. The solvent was removed in vacuo affording 0.57 g of 2-{[2-amino-6-(trifluoromethyl)phenyl]amino}ethanol: MS (ES) m/z 219 [M−H].

後処理

  1. additionwas added
  2. temperatureThe reaction mixture was cooled
  3. concentrationconcentrated in vacuo
  4. extractionThe residue was extracted with ethyl acetate
  5. dry with materialthe organic phase was dried over magnesium sulfate
  6. customThe solvent was removed in vacuo

出典と根拠

ORDレコード
ord-cea36f64a7de4acea5ec0ce77d5b489a
出典データセット
uspto-grants-2010_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07645784B2

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート