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Sodium Carbonate → 4-Amino-3-iodo-n-methylbenzeneacetamide

HRID 1080696
ノート
印刷プレビュー

反応式

HRID 1080696 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH2:8][C:9]([NH:11][CH3:12])=[O:10])=[CH:4][CH:3]=1.[I:13]Cl.C([O-])([O-])=O.[Na+].[Na+]>CC#N>[NH2:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][C:9]([NH:11][CH3:12])=[O:10])=[CH:6][C:7]=1[I:13]
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 10340Sodium CarbonateHCID 24640Iodine chlorideHCID 167753762-(4-aminophenyl)-N-methylacetamide

生成物 1

HCID 233658104-Amino-3-iodo-n-methylbenzeneacetamide収率 63.6%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

4-Amino-N-methyl-benzeneacetamide (6) (6.56 g, 0.04 mol) was dissolved in CH3CN (200 mL) and ICl (7.14 g dissolved in 60 mL of CH3CN, 0.044 mol) was added dropwise with vigorous stirring. After stirring at RT for 3 h, saturated aqueous Na2CO3 (50 mL) was added and the reaction was concentrated in vacuo. The residue was dissolved in EtOAc and extracted with saturated aqueous Na2CO3. The organic phase was dried over MgSO4, filtered and concentrated in vacuo. The product (7) (7.38 g, 63.6%) was isolated from the concentrate by trituration with CH2Cl2 /EtOAc and washing with Et2O. This material was found to be pure by NMR analysis.

後処理

  1. concentrationthe reaction was concentrated in vacuo
  2. dissolutionThe residue was dissolved in EtOAc
  3. extractionextracted with saturated aqueous Na2CO3
  4. dry with materialThe organic phase was dried over MgSO4
  5. filtrationfiltered
  6. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-dc889fbb2693491f9ef6ab0f8193131f
出典データセット
uspto-grants-1996_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05583149

反応ノート

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