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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Lithium hydroxide, monohydrate → HCID 22918353、化合物

HRID 2396040
ノート
印刷プレビュー

反応式

HRID 2396040 の反応式
C[O:2][C:3](=[O:28])[C:4]1[C:5](=[CH:10][C:11]([NH:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)=[C:12]([NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:13]=1)[C:6]([O:8]C)=[O:7].O.[OH-].[Li+]>CO.O>[NH:14]([C:12]1[CH:13]=[C:4]([C:3]([OH:28])=[O:2])[C:5](=[CH:10][C:11]=1[NH:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)[C:6]([OH:8])=[O:7])[C:15]1[CH:16]=[CH:17][CH:18]=[CH:19][CH:20]=1
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 2

HCID 168937Lithium hydroxide, monohydrateHCID 10407176dimethyl 4,5-dianilinobenzene-1,2-dicarboxylate

生成物 1

HCID 22918353HCID 22918353、化合物

試薬・触媒・溶媒 2

HCID 887Methanol溶媒HCID 962Water溶媒2 回

実験手順

A steady stream of argon is passed through a suspension of 26.35 g (70.0 mmol) of 4,5-bis(anilino)phthalic acid dimethylester in 230 ml of methanol, and a solution of 11.78 g (280 mmol, 2 eq) of lithium hydroxide monohydrate in 116 ml of water is added. The reaction mixture is heated toreflux for 2.5 h, cooled to RT and diluted with 400 ml water. Methanol is removed by evaporation, the resulting solution is cooled to 0°, and70 ml 4N hydrochloric acid are added. After 15 min. at 0°, the gray crystals are filtered off, washed with water and resuspended twice in 200 ml toluene with removal of the toluene by distillation to yield the title compound in the form of gray crystals, FAB-MS: 349 [M+ +H].

後処理

  1. temperatureThe reaction mixture is heated
  2. customMethanol is removed by evaporation
  3. temperaturethe resulting solution is cooled to 0°
  4. additionand70 ml 4N hydrochloric acid are added
  5. waitAfter 15 min. at 0°
  6. filtrationthe gray crystals are filtered off
  7. washwashed with water
  8. customresuspended twice in 200 ml toluene with removal of the toluene by distillation

出典と根拠

ORDレコード
ord-928003f90c264307b7f725e9eec4a385
出典データセット
uspto-grants-1996_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05491144

反応ノート

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