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Dipotassium 5-(2-phenylethynyl)isophthalate → 5-(Phenylethynyl)isophthalic acid

HRID 498159
ノート
印刷プレビュー

反応式

HRID 498159 の反応式
[C:1]1([C:7]#[C:8][C:9]2[CH:10]=[C:11]([C:18]([O-:20])=[O:19])[CH:12]=[C:13]([CH:17]=2)[C:14]([O-:16])=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[K+].[K+]>O>[C:1]1([C:7]#[C:8][C:9]2[CH:10]=[C:11]([C:18]([OH:20])=[O:19])[CH:12]=[C:13]([CH:17]=2)[C:14]([OH:16])=[O:15])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 1

HCID 12080907Dipotassium 5-(2-phenylethynyl)isophthalate

生成物 1

HCID 120809085-(Phenylethynyl)isophthalic acid収率 99.5%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

Dipotassium 5-(2-phenylethynyl)isophthalate in an amount of 6.5 g (0.019 moles) was dissolved into 20 ml of ion-exchanged water and insoluble substances were removed by filtration with a 5C filter paper. To the obtained filtrate, a 5 moles/liter hydrochloric acid was added under stirring until the pH became 1. The formed solid substance was separated by filtration, washed with ion-exchanged water and filtered. The filtration and the washing were repeated twice. The obtained solid substance was dried at 50° C. under a reduced pressure and 5.0 g of 5-(2-phenylethynyl)isophthalic acid was obtained (the yield: 99.5%).

後処理

  • customwere removed by filtration with a 5C
  • filtrationfilter paper
  • additionTo the obtained filtrate, a 5 moles/liter hydrochloric acid was added
  • customThe formed solid substance was separated by filtration
  • washwashed with ion-exchanged water
  • filtrationfiltered
  • filtrationThe filtration
  • customThe obtained solid substance was dried at 50° C. under a reduced pressure
  • 出典と根拠

    ORDレコード
    ord-316b86237ff6478c8c843ade2c6feb46
    出典データセット
    uspto-grants-2005_09
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US06949674B2

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