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Stannous Chloride → Methyl 3-amino-4-(methylcarbamoyl)benzoate

HRID 1451114
ノート
印刷プレビュー

反応式

HRID 1451114 の反応式
[CH3:1][NH:2][C:3]([C:5]1[CH:14]=[CH:13][C:8]([C:9]([O:11][CH3:12])=[O:10])=[CH:7][C:6]=1[N+:15]([O-])=O)=[O:4].[Sn](Cl)Cl>C(O)C.O.C(=O)(O)[O-].[Na+]>[NH2:15][C:6]1[CH:7]=[C:8]([CH:13]=[CH:14][C:5]=1[C:3]([NH:2][CH3:1])=[O:4])[C:9]([O:11][CH3:12])=[O:10]
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

6

反応物 2

HCID 24479Stannous ChlorideHCID 10752388Methyl 4-(methylamino)carbonyl-3-nitrobenzoate

生成物 1

HCID 10798400Methyl 3-amino-4-(methylcarbamoyl)benzoate収率 64%

試薬・触媒・溶媒 3

HCID 702Ethanol溶媒HCID 962Water溶媒HCID 516892Sodium Bicarbonate
溶媒

反応条件

温度
70 °C

実験手順

A mixture of methyl 4-(methylamino)carbonyl-3-nitrobenzoate (3.84 g, 0.0185 mol) and tin (ii) chloride (15.3 g, 0.08 mol) in ethanol (80 mL) was heated at 70° C. for 1 h. The reaction mixture was diluted with water (150 mL) and sodium bicarbonate solution was added to it to bring the pH close to 8. The mixture was extracted with ethyl acetate and the organic layer washed with water and brine and dried over sodium sulphate. After filtration, the solution was concentrated and the residue was recrystallized from ethyl acetate-hexane to give 2.16 g (64%) of methyl 3-amino-4-(methylamino)carbonylbenzoate as tan needles, mp 167°-168° C.

後処理

  1. additionwas added to it
  2. customclose to 8
  3. extractionThe mixture was extracted with ethyl acetate
  4. washthe organic layer washed with water and brine
  5. dry with materialdried over sodium sulphate
  6. filtrationAfter filtration
  7. concentrationthe solution was concentrated
  8. customthe residue was recrystallized from ethyl acetate-hexane

出典と根拠

ORDレコード
ord-04ede1a925e0483eb8dc4c4e2a340d0f
出典データセット
uspto-grants-1997_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05602277

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート