Water → Acridine-9-carboxylic acid

HRID 2227790ノート

反応式

HRID 2227790 の反応式
[C:1]([C:3]1[C:4]2[C:9]([N:10]=[C:11]3[C:16]=1[CH:15]=[CH:14][CH:13]=[CH:12]3)=[CH:8][CH:7]=[CH:6][CH:5]=2)#N.N([O-])=[O:18].[Na+].[OH2:21]>S(=O)(=O)(O)O.[OH-].[Na+]>[C:1]([C:3]1[C:4]2[C:9]([N:10]=[C:11]3[C:16]=1[CH:15]=[CH:14][CH:13]=[CH:12]3)=[CH:8][CH:7]=[CH:6][CH:5]=2)([OH:18])=[O:21]

参加物

6

反応物 3

HCID 962WaterHCID 947199-AcridinecarbonitrileHCID 23668193Sodium Nitrite

生成物 1

HCID 94721Acridine-9-carboxylic acid

試薬・触媒・溶媒 2

HCID 1118Sulfuric Acid溶媒HCID 14798Sodium Hydroxide溶媒

反応条件

温度
100 °C

実験手順

Part of the product of the above procedure, that is, 9-cyano acridine (4 g) is dissolved in sulphuric acid containing 10% by weight of distilled water (total volume equals 40 cm3). The mixture thus obtained is heated at a temperature of 100° C. for 2 hours after which time sodium nitrite (10.7 g) is added slowly with continuous stirring. The resulting mixture is heated at 100° C. for 2 hours then poured into cold, distilled water (650 cm3) The solid material which precipitates at this stage is isolated by filtration and allowed to dissolve in the minimum quantity of one molar sodium hydroxide solution; the solution thus obtained is filtered and the filtrate made slightly acidic by the addition of a 50%, by volume, solution of sulphuric acid in water. The 9-carboxy-acridine so formed is then dried in vacuo.

後処理

  1. customThe mixture thus obtained
  2. additionis added slowly with continuous stirring
  3. additionthen poured into cold,
  4. distillationdistilled water (650 cm3) The solid material which
  5. customprecipitates at this stage
  6. customis isolated by filtration
  7. customthe solution thus obtained
  8. filtrationis filtered
  9. additionthe filtrate made slightly acidic by the addition of a 50%, by volume, solution of sulphuric acid in water

出典と根拠

ORDレコード
ord-4eb45db414c8464cb98fac6f9897ecb0
出典データセット
uspto-grants-2002_07
特許番号
US06414152B1

反応ノート

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