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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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Hydrochloric Acid → HCID 15023988、化合物

HRID 1086352
ノート
印刷プレビュー

反応式

HRID 1086352 の反応式
[OH-].[Na+].[CH3:3][O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C:12](=[O:16])[C:13]([OH:15])=[O:14])=[CH:7][CH:6]=1.[CH3:17]I.Cl>CO>[O:16]=[C:12]([CH:11]([C:8]1[CH:7]=[CH:6][C:5]([O:4][CH3:3])=[CH:10][CH:9]=1)[CH3:17])[C:13]([OH:15])=[O:14]
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 4

HCID 313Hydrochloric AcidHCID 6328Methyl iodideHCID 14798Sodium HydroxideHCID 5784733-(4-Methoxyphenyl)-2-oxopropanoic acid

生成物 1

HCID 15023988HCID 15023988、化合物収率 67%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒

実験手順

A 1N aqueous solution of sodium hydroxide (20 ml; 20 mmoles) was slowly added to 1.94 g (10 mmoles) of p-methoxyphenylpyruvic acid and a solution of 1.0 ml of methyl iodide in 50 m 1 of methanol. After addition, the mixture was stirred at room temperature for 4 hours. The mixture was acidified with 1N hydrochloric acid and extracted with three 30 ml portions of ether. The ether layers were dried over magnesium sulfate, and the ether was evaporated under reduced pressure to give a pale yellowish white solid. The NMR spectral analysis of this product led to the determination that this product was nearly pure 2-oxo-3-(p-methoxyphenyl)butanoic acid (1.40 g; yield 67 %).

後処理

  1. additionAfter addition
  2. extractionextracted with three 30 ml portions of ether
  3. dry with materialThe ether layers were dried over magnesium sulfate
  4. customthe ether was evaporated under reduced pressure
  5. customto give a pale yellowish white solid

出典と根拠

ORDレコード
ord-836962916fe64154955bab244a38eb67
出典データセット
uspto-grants-1991_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05028738

反応ノート

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