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Sulfuric Acid → HCID 17930983、化合物

HRID 900439
ノート
印刷プレビュー

反応式

HRID 900439 の反応式
[NH2:1][C:2]1[S:3][C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:5]([C:9]([F:12])([F:11])[F:10])[C:6]=1[C:7]#[N:8].S(=O)(=O)(O)[OH:20].C(=O)(O)[O-].[Na+]>>[NH2:1][C:2]1[S:3][C:4]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)=[C:5]([C:9]([F:10])([F:12])[F:11])[C:6]=1[C:7]([NH2:8])=[O:20]
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

4

反応物 3

HCID 1118Sulfuric AcidHCID 516892Sodium BicarbonateHCID 179309512-Amino-5-phenyl-4-(trifluoromethyl)-3-thiophenecarbonitrile

生成物 1

HCID 17930983HCID 17930983、化合物

反応条件

温度
50 °C

実験手順

A mixture of 2-amino-4-trifluoromethyl-5-phenyl-3-thiophenenitrile (0.12 g) and concentrated sulphuric acid (1.5 ml) was stirred and heated at 50° C. for 8 h. The reaction mixture was added to saturated aqueous sodium bicarbonate until a pH of 7 was obtained. The product was extracted into ethyl acetate (100 ml) and the organic layer was dried with anhydrous sodium sulfate (3 g), filtered and concentrated. The residue was chromatographed on silica gel eluting with ethyl acetate/isohexane mixtures. The solvent was removed and the product collected (0.07 g).

後処理

  1. customwas obtained
  2. extractionThe product was extracted into ethyl acetate (100 ml)
  3. dry with materialthe organic layer was dried with anhydrous sodium sulfate (3 g)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue was chromatographed on silica gel eluting with ethyl acetate/isohexane mixtures
  7. customThe solvent was removed
  8. customthe product collected (0.07 g)

出典と根拠

ORDレコード
ord-eb6ef6370da04431a0d42e3242612ebb
出典データセット
uspto-grants-2008_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07358376B2

反応ノート

読み込み中…

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