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M-Phenylenediamine → HCID 22674043、化合物

HRID 1005671
ノート
印刷プレビュー

反応式

HRID 1005671 の反応式
[C:1]1([NH2:8])[CH:6]=[CH:5][CH:4]=[C:3]([NH2:7])[CH:2]=1.[CH3:9][CH2:10][O:11][C:12]([CH2:14][C:15]([C:17](OCC)=O)=O)=[O:13].P(Cl)(Cl)([Cl:24])=O.[OH-].[Na+]>C(Cl)(Cl)Cl>[NH2:7][C:3]1[CH:2]=[C:1]2[C:6]([C:14]([C:12]([O:11][CH2:10][CH3:9])=[O:13])=[CH:15][C:17]([Cl:24])=[N:8]2)=[CH:5][CH:4]=1
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 4

HCID 7935M-PhenylenediamineHCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 66951Diethyl oxalacetate

生成物 1

HCID 22674043HCID 22674043、化合物

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

To 25 g (231 mmol) of m-phenylenediamine was added 43 g (231 mmol) of diethyl oxaloacetate, followed by stirring at 160 degrees for 1 hour. After standing to cool, the crystals were washed with methanol. To a solution of the crystals (3.0 g, 13 mmol) in chloroform (30 ml) was added phosphorus oxychloride (3.6 ml), followed by heating under reflux for 1 hour. After standing to cool, the reaction mixture was poured onto ice water, basified with 1 N sodium hydroxide aqueous solution, and the resulting crystals were collected by filtration. The crystals were washed with tetrahydrofuran and the filtrate was evaporated, to give 4.85 g of the title compound.

後処理

  1. temperatureto cool
  2. washthe crystals were washed with methanol
  3. temperatureby heating
  4. temperatureunder reflux for 1 hour
  5. temperatureto cool
  6. additionthe reaction mixture was poured onto ice water
  7. filtrationthe resulting crystals were collected by filtration
  8. washThe crystals were washed with tetrahydrofuran
  9. customthe filtrate was evaporated

出典と根拠

ORDレコード
ord-a9cf8abb335e4d9eaf67514f6fff8903
出典データセット
uspto-grants-2004_09
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06787534B2

反応ノート

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