Acetone → HCID 178524616、化合物

HRID 1700783

反応式

HRID 1700783 の反応式
[OH:1][C:2]1[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[C:8]([OH:14])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C(=O)([O-])[O-].[Cs+:19].[Cs+].CC(C)=O>O>[OH:1][C:2]1[CH:10]=[C:9]([C:11]([O-:13])=[O:12])[C:8]([OH:14])=[CH:7][C:3]=1[C:4]([O-:6])=[O:5].[Cs+:19].[Cs+:19]

参加物

5

反応物 3

HCID 180AcetoneHCID 10796Cesium carbonateHCID 691312,5-Dihydroxyterephthalic acid

生成物 1

HCID 178524616HCID 178524616、化合物収率 200%

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

0.5 mol of 2,5-dihydroxyterephthalic acid and 0.5 mol of cesium carbonate were added to 200 ml of acetone and 200 ml of water and dissolved therein by stirring. After completely dissolving, the resultant solution was concentrated to dryness to give 0.5 mol of cesium 2,5-dihydroxyterephthalate. 46.2 g (0.1 mol) of cesium 2,5-dihydroxyterephthalate, 38.62 g (0.2 mol) of bromooctane and 400 ml of DMF were introduced into a reactor and reacted under a nitrogen gas stream at 100° C. for 3 hours. The reaction solution was concentrated, washed with water and dried to give 40.1 g (0.95 mol) of 2,5-dihydroxybenzene-1,6-dicarboxylic octane.

後処理

  1. dissolutiondissolved
  2. dissolutionAfter completely dissolving
  3. concentrationthe resultant solution was concentrated to dryness

出典と根拠

ORDレコード
ord-3eb14a43b8784f7e81ce057f4737fc33
出典データセット
uspto-grants-2002_02
特許番号
US06350845B1

関連ノート

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