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Bromine → Methyl 4-bromo-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate

HRID 274740
ノート
印刷プレビュー

反応式

HRID 274740 の反応式
[Br:1]Br.[Cl:3][C:4]1[CH:9]=[CH:8][C:7]([C:10]2[NH:11][C:12]([C:19]([F:22])([F:21])[F:20])=[CH:13][C:14]=2[C:15]([O:17][CH3:18])=[O:16])=[CH:6][CH:5]=1.C([O-])(=O)C.[Na+]>C(O)(=O)C.S([O-])([O-])=O.[Na+].[Na+]>[Br:1][C:13]1[C:14]([C:15]([O:17][CH3:18])=[O:16])=[C:10]([C:7]2[CH:6]=[CH:5][C:4]([Cl:3])=[CH:9][CH:8]=2)[NH:11][C:12]=1[C:19]([F:22])([F:20])[F:21]
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 24408BromineHCID 517045Sodium AcetateHCID 11034029Methyl 2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate

生成物 1

HCID 20093623Methyl 4-bromo-2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate収率 82.4%

試薬・触媒・溶媒 2

HCID 176Acetic Acid溶媒
HCID 24437
Sodium Sulfite
溶媒

実験手順

Bromine (2.3 mL, 43.7 mmol) is added to a solution of methyl 2-(p-chlorophenyl)-5-(trifluoromethyl)pyrrole-3-carboxylate (8.44 g, 29.2 mmol) and sodium acetate (3.6 g, 43.7 mmol) in acetic acid. The reaction mixture is stirred for 30 minutes, diluted with a 0.4 wt/wt% sodium sulfite solution and extracted with diethyl ether. The organic extracts are combined, washed with saturated sodium hydrogen carbonate solution, dried over anhydrous Na2SO4 and concentrated in vacuo to obtain an oil which solidifies to give the title product as a solid (9.2 g) which is identified by 1H and 13C NMR spectral analyses.

後処理

  1. extractionextracted with diethyl ether
  2. washwashed with saturated sodium hydrogen carbonate solution
  3. dry with materialdried over anhydrous Na2SO4
  4. concentrationconcentrated in vacuo
  5. customto obtain an oil which

出典と根拠

ORDレコード
ord-cbcceaab31b44c629c1fc89c07cd980f
出典データセット
uspto-grants-1995_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05389669

反応ノート

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