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Stannous chloride dihydrate → 2-Amino-4-fluorophenol

HRID 7766
ノート
印刷プレビュー

反応式

HRID 7766 の反応式
[F:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([N+:9]([O-])=O)[CH:3]=1.O.O.[Sn](Cl)Cl.C([O-])(O)=O.[Na+]>CO>[NH2:9][C:4]1[CH:3]=[C:2]([F:1])[CH:7]=[CH:6][C:5]=1[OH:8]
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 61436Stannous chloride dihydrateHCID 1362364-Fluoro-2-nitrophenolHCID 516892Sodium Bicarbonate

生成物 1

HCID 27359172-Amino-4-fluorophenol

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

To a stirred solution of 4-fluoro-2-nitrophenol (4.05 g, 25.8 mmol) in MeOH (200 mL) was added tin(II) chloride dihydrate (17.47 g, 77.4 mmol). The reaction mixture was heated at reflux and monitored by LC/MS. When significant reduction was complete, the reaction mixture was cooled to rt, poured over ice, and made basic (pH 9) with 50% saturated NaHCO3. The aqueous layer was extracted with EtOAc (2×200 mL) and the combined extracts washed with brine, dried over MgSO4, filtered, and concentrated in vacuo to give 2-amino-4-fluorophenol as a grayish green solid. 1H NMR (CDCl3, 300 MHz) δ 6.64 (dd, 1H), 6.47 (dd, 1H), 6.33 (dt, 1H), 4.48 (br s, 1H), 3.78 (br s, 2H).

後処理

  1. temperatureThe reaction mixture was heated
  2. temperatureat reflux
  3. additionpoured over ice
  4. extractionThe aqueous layer was extracted with EtOAc (2×200 mL)
  5. washthe combined extracts washed with brine
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-155edca81d244fa58d3afef51264be52
出典データセット
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07087601B2

反応ノート

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