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Ethanol → HCID 57562941、化合物

HRID 2408369
ノート
印刷プレビュー

反応式

HRID 2408369 の反応式
[NH2:1][S:2]([C:5]1[CH:6]=[C:7]([N+:13]([O-])=O)[CH:8]=[C:9]([CH3:12])[C:10]=1[F:11])(=[O:4])=[O:3].C(O)C.[Cl-].[NH4+]>[Fe].O>[NH2:1][S:2]([C:5]1[CH:6]=[C:7]([CH:8]=[C:9]([CH3:12])[C:10]=1[F:11])[NH2:13])(=[O:4])=[O:3]
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

6

反応物 3

HCID 702EthanolHCID 25517Ammonium ChlorideHCID 57562895HCID 57562895、化合物

生成物 1

HCID 57562941HCID 57562941、化合物

試薬・触媒・溶媒 2

HCID 23925Iron触媒HCID 962Water溶媒

反応条件

温度
60 °C

実験手順

To a heterogeneous solution of 3-aminosulfonyl-4-fluoro-5-methylnitrobenzene (27) (0.5 g, 2 mmol) in of ethanol:water (50 mL, each) were added iron powder (1.08 g, 20 mmol), and ammonium chloride (1.08 g, 20 mmol) at room temperature. The resulting heterogeneous mixture was then stirred at 60° C. for 2 hours, filtered through celite (when hot), washed with ethanol (2×50 mL) and then the solvent was removed under reduced pressure. The residue upon dilution with water was extracted with ethyl acetate (3×50 mL), and the organic phase was dried over anhydrous sodium sulfate and concentrated under a reduced pressure to obtain 3-aminosulfonyl-4-fluoro-5-methylaniline (28). LCMS: purity: 85%; MS (m/z): 205 (MH+).

後処理

  1. filtrationfiltered through celite (when hot)
  2. washwashed with ethanol (2×50 mL)
  3. customthe solvent was removed under reduced pressure
  4. extractionThe residue upon dilution with water was extracted with ethyl acetate (3×50 mL)
  5. dry with materialthe organic phase was dried over anhydrous sodium sulfate
  6. concentrationconcentrated under a reduced pressure

出典と根拠

ORDレコード
ord-a5cfbe0bc28d453db3562db5a03032cf
出典データセット
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08815848B2

反応ノート

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