Anthraquinone → 9,10-Anthracenediol

HRID 1180326

反応式

HRID 1180326 の反応式
[OH-].[Na+].[CH:3]1[C:16]2[C:15](=[O:17])[C:14]3[C:9](=[CH:10][CH:11]=[CH:12][CH:13]=3)[C:8](=[O:18])[C:7]=2[CH:6]=[CH:5][CH:4]=1.[Na:19].OC1C2C(C(O)=C3C=1CC=CC3)=CC=CC=2.C1(=O)C2C(=CC3C(C=2)=CC=CC=3)C=CC1=O>O>[Na:19].[CH:10]1[C:9]2[C:14](=[C:15]([OH:17])[C:16]3[C:7]([C:8]=2[OH:18])=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH:13]=[CH:12][CH:11]=1

参加物

8

反応物 5

HCID 6780AnthraquinoneHCID 14798Sodium HydroxideHCID 920209,10-Anthracenediol, 1,4-dihydro-HCID 101219AnthracenedioneHCID 5360545Sodium

生成物 2

HCID 210829,10-AnthracenediolHCID 5360545Sodium

試薬・触媒・溶媒 1

HCID 962Water溶媒

反応条件

温度
87.5 °C

実験手順

A three necked flask having a capacity of 300 ml and equipped with a stirrer, a thermometer, a heating jacket and a charge inlet, 32 g of a 30% sodium hydroxide aqueous solution and 57 g of water were charged, and with stirring, 25 g of 9,10-anthracenedione was charged and suspended, whereupon air in the flask was substituted by nitrogen. While stirring the content in this flask, 130 g of an aqueous solution of a sodium salt of 1,4-dihydro-9,10-dihydroxyanthracene (22% as the concentration of anthracenedione) was added, and the mixture was maintained at an internal temperature within a range of from 85 to 90° C. for 4 hours to obtain an aqueous solution of a sodium salt of 9,10-anthracenediol.

後処理

  1. customequipped with a stirrer
  2. stirringWhile stirring the content in this flask

出典と根拠

ORDレコード
ord-6812c3b188b24fa587c87b32dcc62f1b
出典データセット
uspto-grants-2007_10
特許番号
US07279607B2

関連ノート

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