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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 12750106、化合物

HRID 725732
ノート
印刷プレビュー

反応式

HRID 725732 の反応式
[CH2:1]([C:5]1[CH:11]=[CH:10][C:8]([NH2:9])=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].[C:12](OC(=O)C)(=[O:14])[CH3:13].O>C(O)(=O)C>[CH2:1]([C:5]1[CH:6]=[CH:7][C:8]([NH:9][C:12](=[O:14])[CH3:13])=[CH:10][CH:11]=1)[CH:2]([CH3:4])[CH3:3]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 7918Acetic AnhydrideHCID 1216274-Isobutylaniline

生成物 1

HCID 12750106HCID 12750106、化合物収率 67.3%

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

70.0 g (0.47 mol) of p-isobutylaniline was dissolved in 126 ml of glacial acetic acid. 59.9 g (0.58 mol) of acetic anhydride was then added dropwise to the solution at a temperature of 30° C. After the completion of dropwise addition, the reaction mixture was then allowed to undergo reaction at a temperature of 40° C. for 1 hour. The reaction solution was then poured into 500 ml of water. The resulting crystal was filtered off, washed with water, and then dried. The crystal thus obtained was then recrystallized from a mixture of 140 ml of toluene and 700 ml of n-hexane to obtain 60.4 g (yield: 67.3%) of p-isobutylacetanilide. The melting point of the crystal was from 124.5° C. to 125.0° C.

後処理

  1. additionAfter the completion of dropwise addition
  2. customreaction at a temperature of 40° C. for 1 hour
  3. filtrationThe resulting crystal was filtered off
  4. washwashed with water
  5. customdried
  6. customThe crystal thus obtained
  7. customwas then recrystallized from a mixture of 140 ml of toluene and 700 ml of n-hexane

出典と根拠

ORDレコード
ord-b25d05fb269f4dd99484ab1594944e33
出典データセット
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05707747

反応ノート

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