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Acetic Acid → N-(2-Amino-4-bromophenyl)-2-chloroacetamide

HRID 44186
ノート
印刷プレビュー

反応式

HRID 44186 の反応式
[Cl-].[NH4+].C(O)(=O)C.[Br:7][C:8]1[CH:13]=[CH:12][C:11]([NH:14][C:15](=[O:18])[CH2:16][Cl:17])=[C:10]([N+:19]([O-])=O)[CH:9]=1.C(=O)([O-])[O-].[Na+].[Na+]>O.CN(C=O)C>[NH2:19][C:10]1[CH:9]=[C:8]([Br:7])[CH:13]=[CH:12][C:11]=1[NH:14][C:15](=[O:18])[CH2:16][Cl:17]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

HCID 176Acetic AcidHCID 10340Sodium CarbonateHCID 25517Ammonium ChlorideHCID 16457083N-(4-bromo-2-nitrophenyl)-2-chloroacetamide

生成物 1

HCID 66911433N-(2-Amino-4-bromophenyl)-2-chloroacetamide収率 43.3%

試薬・触媒・溶媒 2

HCID 962Water溶媒
HCID 6228Dimethylformamide溶媒

反応条件

温度
50 °C

実験手順

Ferrous powder (19.8 g, 354 mmol), ammonium chloride (1.1 g, 19.7 mmol) and acetic acid (4.9 ml, 86.5 mmol) were suspended in 300 ml water and stirred at 50° C. for 15 min. To this mixture, a solution of N-(4-bromo-2-nitrophenyl)-2-chloroacetamide (11.5 g, 39.3 mmol) in 100 ml DMF was added quickly. After stirring for 15 min, the mixture was basified to pH 9 with aqueous sodium carbonate solution. The remaining solids were filtered and washed with water and ethyl acetate. Extraction of the water layer with ethyl acetate, washing of the combined organic layers with brine, drying over MgSO4, removing the solvent under reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1) yielded N-(2-amino-4-bromophenyl)-2-chloroacetamide (4.5 g, 17.0 mmol, 43%) as an off-white solid.

後処理

  1. stirringAfter stirring for 15 min
  2. filtrationThe remaining solids were filtered
  3. washwashed with water and ethyl acetate
  4. extractionExtraction of the water layer with ethyl acetate
  5. washwashing of the combined organic layers with brine
  6. dry with materialdrying over MgSO4
  7. customremoving the solvent
  8. customunder reduced pressure and purification of the crude product by flash chromatography on silica gel (petroleum ether/ethyl acetate, 1/1)

出典と根拠

ORDレコード
ord-43f833b971914c87909b782e12612778
出典データセット
uspto-grants-2013_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08541404B2

反応ノート

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