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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
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Water → HCID 12789562、化合物

HRID 1732724
ノート
印刷プレビュー

反応式

HRID 1732724 の反応式
[C:1](=[O:4])([O-])[O-:2].[K+].[K+].[OH:7][C:8]1[CH:18]=[CH:17][C:11]([C:12]([O:14][CH2:15][CH3:16])=[O:13])=[CH:10][CH:9]=1.O>[N+](C1C=CC=CC=1)([O-])=O.[Cu]>[CH2:15]([O:14][C:12]([C:11]1[CH:10]=[CH:9][C:8]([O:7][C:8]2[CH:18]=[CH:17][CH:11]=[CH:10][C:9]=2[C:1]([OH:2])=[O:4])=[CH:18][CH:17]=1)=[O:13])[CH3:16]
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 3

HCID 962WaterHCID 8434EthylparabenHCID 11430Potassium Carbonate2 回

生成物 1

HCID 12789562HCID 12789562、化合物収率 145.5%

試薬・触媒・溶媒 2

HCID 23978Copper触媒HCID 7416Nitrobenzene溶媒

実験手順

Potassium carbonate (14 g) was added to a solution of 2-indobenzoic acid (50 g) in nitrobenzene (50 ml) at 140°-150° C. with stirring. The mixture was stirred for an additional 10 minutes after the addition. Then, ethyl 4-hydroxybenzoate (33.5 g), potassium carbonate (28 g) and copper (3 g) were added. The mixture was stirred at 150°-160° C. for 30 minutes and allowed to cool. After the addition of water, the mixture was filtered and the filtrate was acidified with concentrated hydrochloric acid. The precipitate was collected and recrystallized from dilute ethanol to give the title compound (42 g, 72%), m.p. 152°-153° C.

後処理

  1. stirringThe mixture was stirred for an additional 10 minutes
  2. additionafter the addition
  3. stirringThe mixture was stirred at 150°-160° C. for 30 minutes
  4. temperatureto cool
  5. filtrationthe mixture was filtered
  6. customThe precipitate was collected
  7. customrecrystallized from dilute ethanol

出典と根拠

ORDレコード
ord-54dc4baba703474e939a09dbe855f6fd
出典データセット
uspto-grants-1980_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04238620

反応ノート

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