Methylamine → 5-Methylsulfamoyl-2-trifluoromethoxy-benzoic acid

HRID 225710ノート

反応式

HRID 225710 の反応式
Cl[S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:14][C:15]([F:18])([F:17])[F:16])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3].[CH3:19][NH2:20]>ClCCl.CO>[CH3:19][NH:20][S:2]([C:5]1[CH:6]=[CH:7][C:8]([O:14][C:15]([F:18])([F:17])[F:16])=[C:9]([CH:13]=1)[C:10]([OH:12])=[O:11])(=[O:4])=[O:3]

参加物

5

実験手順

To a solution of 5-Chlorosulfonyl-2-trifluoromethoxy-benzoic acid (0.15 g) in dichloromethane (1.5 ml) was added a solution of methylamine in methanol (8M, 0.31 mL) and the reaction mixture was stirred for 2 minutes after precipitation was compete. The reaction mixture was then concentrated in vacuo and the residue was dissolved in 1N NaOH (2 mL) and extracted with diethylether. The aqueous phase was then acidified using 3 N hydrochloric acid solution (2 mL) and the solution was extracted with dichloromethane (2×10 mL). The combined organic phases were dried with sodium sulfate and concentrated in vacuo to yield the title compound as a white solid (0.12 g). MS (m/e): 298.0 (M−H, 100%).

後処理

  1. customafter precipitation
  2. concentrationThe reaction mixture was then concentrated in vacuo
  3. dissolutionthe residue was dissolved in 1N NaOH (2 mL)
  4. extractionextracted with diethylether
  5. extractionthe solution was extracted with dichloromethane (2×10 mL)
  6. dry with materialThe combined organic phases were dried with sodium sulfate
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-95023419463a4593ae2e96f46e223dc7
出典データセット
uspto-grants-2009_07
特許番号
US07557114B2

反応ノート

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