ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
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
  1. ホーム
  2. /反応

Hydrochloric Acid → 2-Methoxy-4-(methylamino)-5-nitrobenzoic acid

HRID 2293532
ノート
印刷プレビュー

反応式

HRID 2293532 の反応式
Cl[C:2]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[C:4]([O:14][CH3:15])[CH:3]=1.[OH-].[Na+].Cl.CO.[CH3:21][NH2:22]>>[CH3:15][O:14][C:4]1[CH:3]=[C:2]([NH:22][CH3:21])[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][C:5]=1[C:6]([OH:8])=[O:7]
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 4

HCID 313Hydrochloric AcidHCID 14798Sodium HydroxideHCID 128487494-Chloro-2-methoxy-5-nitrobenzoic acidHCID 57454252Monomethylamine methanol

生成物 1

HCID 109879372-Methoxy-4-(methylamino)-5-nitrobenzoic acid

実験手順

A 1.00 g portion of 4-chloro-2-methoxy-5-nitrobenzoic acid and 0.52 g of sodium hydroxide were dissolved in 20 ml of 40% methylamine methanol solution, followed by stirring at room temperature for 12 hours. After completion of the reaction, the reaction solution was poured on crushed ice and adjusted to pH 4 with 6N hydrochloric acid aqueous solution. The thus precipitated product of interest was collected by filtration, washed with water and dried under a reduced pressure and then the resulting crude product was purified by silica gel column chromatography (chloroform:methanol=20:1) to give 0.30 g of 2-methoxy-4-methylamino-5-nitrobenzoic acid.

後処理

  1. customAfter completion of the reaction
  2. additionthe reaction solution was poured
  3. customon crushed ice
  4. filtrationThe thus precipitated product of interest was collected by filtration
  5. washwashed with water
  6. customdried under a reduced pressure
  7. customthe resulting crude product was purified by silica gel column chromatography (chloroform:methanol=20:1)

出典と根拠

ORDレコード
ord-c215394ecce14f8f86158ae691998e20
出典データセット
uspto-grants-1997_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05686482

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート