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Sodium Hydroxide → HCID 12897089、化合物

HRID 1980944
ノート
印刷プレビュー

反応式

HRID 1980944 の反応式
[Cl:1][C:2]1[NH:6][CH:5]=[C:4]([C:7]([O:9]C)=[O:8])[CH:3]=1.[OH-].[Na+]>CO>[Cl:1][C:2]1[NH:6][CH:5]=[C:4]([C:7]([OH:9])=[O:8])[CH:3]=1
参加物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 12897088HCID 12897088、化合物

生成物 1

HCID 12897089HCID 12897089、化合物

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

Methyl 5-chloropyrrole-3-carboxylate (900 g.) was refluxed for 9 hours with 20 ml. of methanol and 10 ml. of 1N sodium hydroxide. Methanol was removed by evaporation, the aqueous residue was diluted with approximately 10 ml. of water and extracted twice with ether. The aqueous phase was acidified with conc. hydrochloric acid and product extracted into ethyl acetate. The three ethyl acetate extracts were combined, washed with saturated sodium chloride, dried over anhydrous sodium sulfate and evaporated to product (715 mg., m.p. 175°-178° C.). Recrystallization from methylene chloride/hexane afforded purified 5-chloropyrrole-3-carboxylic acid (300 mg., m.p. 178°-180° C.).

後処理

  1. customMethanol was removed by evaporation
  2. additionthe aqueous residue was diluted with approximately 10 ml
  3. extractionof water and extracted twice with ether
  4. extractionextracted into ethyl acetate
  5. washwashed with saturated sodium chloride
  6. dry with materialdried over anhydrous sodium sulfate
  7. customevaporated to product (715 mg., m.p. 175°-178° C.)
  8. customRecrystallization from methylene chloride/hexane
  9. customafforded
  10. custompurified 5-chloropyrrole-3-carboxylic acid (300 mg., m.p. 178°-180° C.)

出典と根拠

ORDレコード
ord-127a07f7ded140cc8184d55e524c58ea
出典データセット
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04511575

反応ノート

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