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Chloroacetyl chloride → 2-chloro-N-(2,6-dihydroxyphenyl)acetamide

HRID 2112743
ノート
印刷プレビュー

反応式

HRID 2112743 の反応式
OP([O-])(O)=O.[K+].OP([O-])([O-])=O.[K+].[K+].[NH2:14][C:15]1[C:20]([OH:21])=[CH:19][CH:18]=[CH:17][C:16]=1[OH:22].[Cl:23][CH2:24][C:25](Cl)=[O:26]>O>[Cl:23][CH2:24][C:25]([NH:14][C:15]1[C:20]([OH:21])=[CH:19][CH:18]=[CH:17][C:16]=1[OH:22])=[O:26]
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 6577Chloroacetyl chlorideHCID 24450Potassium Phosphate, DibasicHCID 694512-AminoresorcinolHCID 516951Monobasic potassium phosphate

生成物 1

HCID 100815492-chloro-N-(2,6-dihydroxyphenyl)acetamide

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

KH2PO4 (17.2 g, 126.3 mmol) and K2HPO4 (8.2 g, 35.7 mmol) in 188 ml of distilled water were deoxygenated by passing argon through the mixture for 0.5 hour. 2-Aminobenzene-1,3-diol (1 g, 8.0 mmol) was added to the buffer solution and chloroacetyl chloride (0.64 ml, 8.0 mmol) was added slowly to the reaction mixture. After addition was completed, the reaction mixture was stirred at room temperature for 1.5 hours. Water was removed by freeze-drying and the residue was dissolved in 20% MeOH in DCM. The insoluble salt was removed by filtration, the solvent was evaporated to give the subtitled compound which was used without purification in the next step.

後処理

  1. customfor 0.5 hour
  2. additionwas added slowly to the reaction mixture
  3. additionAfter addition
  4. customWater was removed
  5. customby freeze-drying
  6. dissolutionthe residue was dissolved in 20% MeOH in DCM
  7. customThe insoluble salt was removed by filtration
  8. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-c4cd83cdff0343a0aeafbea1c738f57c
出典データセット
uspto-grants-2009_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07524856B2

反応ノート

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