Acetic Anhydride → 1,3-Dimethyl-1H-indazole-4,5-dicarboxylic anhydride

HRID 439727

反応式

HRID 439727 の反応式
[CH3:1][N:2]1[C:10]2[C:5](=[C:6]([C:14]([OH:16])=[O:15])[C:7]([C:11](O)=[O:12])=[CH:8][CH:9]=2)[C:4]([CH3:17])=[N:3]1.C(OC(=O)C)(=O)C>>[CH3:1][N:2]1[C:10]2[C:5](=[C:6]3[C:14](=[O:16])[O:15][C:11](=[O:12])[C:7]3=[CH:8][CH:9]=2)[C:4]([CH3:17])=[N:3]1

参加物

3

反応物 2

HCID 7918Acetic AnhydrideHCID 224029461,3-dimethyl-1H-indazole-4,5-dicarboxylic acid

生成物 1

HCID 541895841,3-Dimethyl-1H-indazole-4,5-dicarboxylic anhydride

反応条件

温度
5 °C

実験手順

A mixture of 1,3-dimethyl-1H-indazole-4,5-dicarboxylic acid (6.30 g, 26.9 mmol) and acetic anhydride is stirred at reflux temperature for 3 hours, cooled to 5° C. and filtered. The filter cake is air-dried to give the title product as chartreuse needles (4.80 g, 82.5%), mp 214°-215.5° C.

後処理

  1. temperatureat reflux temperature for 3 hours
  2. filtrationfiltered
  3. customThe filter cake is air-dried

出典と根拠

ORDレコード
ord-78e7a39351404ae2a23594c95eb484cf
出典データセット
uspto-grants-1996_05
特許番号
US05516751

関連ノート

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