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Methanol → 1-Methanesulfonyl-5-methoxy-phenylamine

HRID 418076
ノート
印刷プレビュー

反応式

HRID 418076 の反応式
[CH3:1][S:2]([C:5]1[CH:10]=[C:9]([N+]([O-])=O)[CH:8]=[C:7]([O:14][CH3:15])[CH:6]=1)(=[O:4])=[O:3].[Cl-].[NH4+:17].CO>[Zn].O>[CH3:1][S:2]([C:5]1([NH2:17])[CH:6]=[C:7]([O:14][CH3:15])[CH:8]=[CH:9][CH2:10]1)(=[O:4])=[O:3]
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 887MethanolHCID 25517Ammonium ChlorideHCID 578630801-(Methanesulfonyl)-3-methoxy-5-nitrobenzene

生成物 1

HCID 666496371-Methanesulfonyl-5-methoxy-phenylamine収率 76%

試薬・触媒・溶媒 2

HCID 23994Zinc触媒HCID 962Water溶媒2 回

実験手順

To a mixture of 1-methanesulfonyl-3-methoxy-5-nitro-benzene (1.5 g, 6.48 mmol), zinc dust (4.3 g, 64.87 mmol), and ammonium chloride (5.2 g, 97.31 mmol) were added methanol (20.32 mL) and water (9.9 mL) at room temperature. After addition of water, the reaction was exothermic. The suspension was stirred for 30 min and the reaction mixture was filtered through the Celite. The filter cake was washed with water and methanol. The filtrate was concentrated to remove methanol and the residue was extracted with ethyl acetate (2×50 mL). The combined extracts were washed with brine solution (100 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo to isolate 1-methanesulfonyl-5-methoxy-phenylamine (1.0 g, 76%) as a light yellow solid: ES(+)-HRMS m/e calcd for C8H12NO3S (M+H)+ 202.0533, found 202.0532.

後処理

  1. filtrationthe reaction mixture was filtered through the Celite
  2. washThe filter cake was washed with water and methanol
  3. concentrationThe filtrate was concentrated
  4. customto remove methanol
  5. extractionthe residue was extracted with ethyl acetate (2×50 mL)
  6. washThe combined extracts were washed with brine solution (100 mL)
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-e5198d1f0cc34967ab0f6e775fe13335
出典データセット
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08093253B2

反応ノート

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