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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 → 2-(2,4,5-Trimethylphenyl)acetic acid

HRID 1635903
ノート
印刷プレビュー

反応式

HRID 1635903 の反応式
S(=O)(=O)(O)[OH:2].[CH3:6][C:7]1[CH:15]=[C:14]([CH3:16])[C:13]([CH3:17])=[CH:12][C:8]=1[CH2:9][C:10]#N.[OH2:18]>>[CH3:6][C:7]1[CH:15]=[C:14]([CH3:16])[C:13]([CH3:17])=[CH:12][C:8]=1[CH2:9][C:10]([OH:2])=[O:18]
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 3

HCID 962WaterHCID 1118Sulfuric Acid2 回HCID 1447272,4,5-Trimethylphenylacetonitrile

生成物 1

HCID 2989242-(2,4,5-Trimethylphenyl)acetic acid収率 90%

反応条件

温度
90 °C

実験手順

2118 ml of concentrated sulphuric acid are added dropwise to 2662 ml of water at room temperature and the solution is heated to 90° C. 355 g (2.23 mol) of 2,4,5-trimethyl-benzyl cyanide are metered into the half-concentrated sulphuric acid at this temperature and the mixture is subsequently stirred at 100° C. for 8 hours. After cooling, the reaction mixture is poured into ice-water, while stirring vigorously, and filtered with suction. The solid is washed several times with water and then with petroleum ether and dried. 358 g (90% of theory) of 2,4,5-trimethylphenylacetic acid having a melting point of 123-125° C. are obtained.

後処理

  1. temperatureAfter cooling
  2. stirringwhile stirring vigorously
  3. filtrationfiltered with suction
  4. washThe solid is washed several times with water
  5. dry with materialwith petroleum ether and dried

出典と根拠

ORDレコード
ord-cfd4af4b8c054b8ea06d1bd88d5aef25
出典データセット
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06511942B1

反応ノート

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このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート