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3-Aminophenol → 3-Hydrazinylphenol

HRID 2200048
ノート
印刷プレビュー

反応式

HRID 2200048 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1.[N:9]([O-])=O.[Na+].[Sn](Cl)Cl>Cl.O>[NH:1]([C:2]1[CH:3]=[C:4]([OH:8])[CH:5]=[CH:6][CH:7]=1)[NH2:9]
参加物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 115683-AminophenolHCID 24479Stannous ChlorideHCID 23668193Sodium Nitrite

生成物 1

HCID 143447513-Hydrazinylphenol収率 16%

試薬・触媒・溶媒 2

HCID 313Hydrochloric Acid溶媒2 回HCID 962Water溶媒

実験手順

To a stirred, ice cooled solution of 3-aminophenol (2.00 g, 18.3 mmol) in concentrated HCl (20 mL) was added dropwise a solution of sodium nitrite (1.33 g, 19.24 mmol) in H2O (10 mL), ensuring the internal temperature did not exceed 10° C. After 10 min, a solution of tin (II) chloride (7.645 g, 40.3 mmol) in concentrated HCl (10 mL) was added dropwise, and the ice bath removed. After stirring at RT for 45 min, the reaction was basified to pH 10 with careful addition of 10 M NaOH solution (50 mL), and then extracted with EtOAc (3×). The organic extracts were dried over MgSO4, concentrated in vacuo and triturated with Et2O to afford the title compound as a brown solid (353 mg, 16%). 1H NMR (300 MHz, d6-DMSO): 3.83 (2H, br s), 5.96-6.02 (1H, m), 6.15-6.21 (1H, m), 6.22 (1H, t, J=2.2 Hz), 6.52 (1H, br s), 6.84 (1H, t, J=8.0 Hz), 8.91 (1H, br s).

後処理

  1. customdid not exceed 10° C
  2. customthe ice bath removed
  3. additionthe reaction was basified to pH 10 with careful addition of 10 M NaOH solution (50 mL)
  4. extractionextracted with EtOAc (3×)
  5. dry with materialThe organic extracts were dried over MgSO4
  6. concentrationconcentrated in vacuo
  7. customtriturated with Et2O

出典と根拠

ORDレコード
ord-2a81ce3658ed472babfe98ac360fbbcc
出典データセット
uspto-grants-2016_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09359354B2

反応ノート

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