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Water → 5-(Methoxymethyl)pyridine-2,3-dicarboxylic acid

HRID 1768746
ノート
印刷プレビュー

反応式

HRID 1768746 の反応式
[CH3:1][O-:2].[Na+].O.[OH-].[Na+].[Br-].[C:8]([C:11]1[CH:12]=[C:13]([CH2:20][N+](C)(C)C)[CH:14]=[N:15][C:16]=1[C:17]([OH:19])=[O:18])([OH:10])=[O:9]>CO>[CH3:1][O:2][CH2:20][C:13]1[CH:12]=[C:11]([C:8]([OH:10])=[O:9])[C:16]([C:17]([OH:19])=[O:18])=[N:15][CH:14]=1
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 962WaterHCID 14798Sodium HydroxideHCID 10942334Sodium MethoxideHCID 111309633-Pyridinemethanaminium, 5,6-dicarboxy-N,N,N-trimethyl-, bromide

生成物 1

HCID 109983115-(Methoxymethyl)pyridine-2,3-dicarboxylic acid

試薬・触媒・溶媒 1

HCID 887Methanol溶媒2 回

実験手順

A mixture of 25% sodium methoxide in methanol (270 g, 1.25 mol) and [(5,6-dicarboxy-3-pyridyl)methyl]trimethylammonium bromide, dimethyl ester (347 g, 1.00 mol) in methanol (650 mL) is heated at reflux for 1 hour under nitrogen. Water (1 L) and sodium hydroxide (80.0 g, 2.0 mol) are added and the reaction mixture is distilled until the pot is 100°-105° C. The reaction mixture is cooled to room temperature, treated with sulfuric acid to adjust the pH to a value from 1.5 to 2 and filtered to obtain a solid. The solid is washed with water and dried in a vacuum oven to obtain the title product as a white solid (mp 161°-162° C.) which is greater than 99% pure by HPLC analysis.

後処理

  1. temperatureis heated
  2. temperatureat reflux for 1 hour under nitrogen
  3. distillationthe reaction mixture is distilled until the
  4. custompot is 100°-105° C
  5. additiontreated with sulfuric acid
  6. filtrationfiltered
  7. customto obtain a solid
  8. washThe solid is washed with water
  9. customdried in a vacuum oven

出典と根拠

ORDレコード
ord-7113bb069f73425c94384580cf6723e2
出典データセット
uspto-grants-1995_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05378843

反応ノート

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