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Sodium Hydroxide → 5-Nitroindole-2-carboxylic acid

HRID 1829985
ノート
印刷プレビュー

反応式

HRID 1829985 の反応式
C([C:3]1[C:11]2[C:6](=[CH:7][CH:8]=[C:9]([N+:12]([O-:14])=[O:13])[CH:10]=2)[NH:5][C:4]=1[C:15]([OH:17])=[O:16])C.[OH-].[Na+]>C(O)C>[N+:12]([C:9]1[CH:10]=[C:11]2[C:6](=[CH:7][CH:8]=1)[NH:5][C:4]([C:15]([OH:17])=[O:16])=[CH:3]2)([O-:14])=[O:13]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 9499843-Ethyl-5-nitro-1H-indole-2-carboxylic acid

生成物 1

HCID 3512915-Nitroindole-2-carboxylic acid

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

反応条件

温度
60 °C

実験手順

To a solution of commercial ethyl 5-Nitro-2-carboxy-indole (10.21 g, 43.6 mmol) in ethanol (220 mL) was added 110 mL of 2 M NaOH. The reaction was stirred at 60° C. for 18 hours. The reaction was then cooled and the ethanol removed in vacuo and then an additional 200 mL water was added. To the vigourously stirring aqueous solution was added 5 M HCl followed by 1 M HCl until pH 4 was attained and the acid product was precipitated. The product was collected by filtration on a Buchner funnel and washed once with dilute HCl (1:40 v/v) and twice with water. The filtrate was dried over P2O5 in a dessicator in vacuo to afford 8.83 g (42.8, 98%) of acid 97.

後処理

  1. temperatureThe reaction was then cooled
  2. customthe ethanol removed in vacuo
  3. additionan additional 200 mL water was added
  4. additionTo the vigourously stirring aqueous solution was added 5 M HCl
  5. customthe acid product was precipitated
  6. filtrationThe product was collected by filtration on a Buchner funnel
  7. washwashed once with dilute HCl (1:40 v/v) and twice with water
  8. dry with materialThe filtrate was dried over P2O5 in a dessicator in vacuo

出典と根拠

ORDレコード
ord-a4f06e4e53304dbb81cd9b17d98d2903
出典データセット
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07064218B2

反応ノート

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