ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Acetic Acid → Pyrogallol triacetate

HRID 1680761
ノート
印刷プレビュー

反応式

HRID 1680761 の反応式
[C:1]1(=NO)[CH2:6][CH2:5][CH2:4][C:3](=NO)[C:2]1=[O:9].[C:12]([OH:15])(=[O:14])[CH3:13].[C:16]([O:19]C(=O)C)(=[O:18])[CH3:17].N1[CH:28]=[CH:27]C=CC=1.[OH2:29]>>[C:12]([O:15][C:1]1[CH:6]=[CH:5][CH:4]=[C:3]([O:19][C:16](=[O:18])[CH3:17])[C:2]=1[O:9][C:27](=[O:29])[CH3:28])(=[O:14])[CH3:13]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 5

HCID 176Acetic Acid2 回HCID 962Water2 回HCID 1049PyridineHCID 7918Acetic AnhydrideHCID 68261391,2,3-Cyclohexanetrione, 1,3-dioxime

生成物 1

HCID 10678Pyrogallol triacetate収率 0.5%

実験手順

To cyclohexane-1,2,3-trione 1,3-dioxime (100 parts) were added glacial acetic acid (400 parts) and water (1600 parts) and the mixture refluxed for four hours at 100°-100.5° C. The pyrogallol was extracted and purified as follows. 47.3% NaOH solution (483 parts) was added to the cooled mixture, when the pH rose from 3.4 to 6.0. The mixture was filtered giving insolubles (60 parts), and the filtrate was continuously extracted with ether. The extract was dried over Na2SO4 and evaporated. The residue was triturated with water and the mixture filtered giving insolubles (8 parts) and a filtrate which was evaporated on a water bath to give a tar (8 parts). To this tar were added glacial acetic acid (42 parts) and acetic anhydride (70 parts) and a catalytic amount of pyridine. After standing at room temperature for five hours, the mixture was drowned out in water and the tar obtained recrystallised from methanol (8 parts) to give pyrogallol triacetate (1 part), melting point 161°-163° C., (0.5% yield).

後処理

  1. temperaturethe mixture refluxed for four hours at 100°-100.5° C
  2. extractionThe pyrogallol was extracted
  3. custompurified
  4. addition47.3% NaOH solution (483 parts) was added to the cooled mixture, when the pH
  5. filtrationThe mixture was filtered
  6. customgiving insolubles (60 parts)
  7. extractionthe filtrate was continuously extracted with ether
  8. dry with materialThe extract was dried over Na2SO4
  9. customevaporated
  10. customThe residue was triturated with water
  11. filtrationthe mixture filtered
  12. customgiving insolubles (8 parts)
  13. customa filtrate which was evaporated on a water bath
  14. customto give a tar (8 parts)
  15. customthe tar obtained
  16. customrecrystallised from methanol (8 parts)

出典と根拠

ORDレコード
ord-dcefd63704d9494bb5320c57d376a114
出典データセット
uspto-grants-1981_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04275247

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート