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Nitric Acid → 2,4-Dimethoxy-5-nitrobenzoic acid

HRID 2293530
ノート
印刷プレビュー

反応式

HRID 2293530 の反応式
[CH3:1][O:2][C:3]1[CH:11]=[C:10]([O:12][CH3:13])[CH:9]=[CH:8][C:4]=1[C:5]([OH:7])=[O:6].[N+:14]([O-])([OH:16])=[O:15]>S(=O)(=O)(O)O>[CH3:1][O:2][C:3]1[CH:11]=[C:10]([O:12][CH3:13])[C:9]([N+:14]([O-:16])=[O:15])=[CH:8][C:4]=1[C:5]([OH:7])=[O:6]
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 944Nitric AcidHCID 70522,4-Dimethoxybenzoic acid

生成物 1

HCID 133076602,4-Dimethoxy-5-nitrobenzoic acid

試薬・触媒・溶媒 1

HCID 1118Sulfuric Acid溶媒

実験手順

(Alternative method) A 2.00 g portion of 2,4-dimethoxybenzoic acid was dissolved in 30 ml of sulfuric acid, and 0.49 ml of concentrated nitric acid was added under ice-cooling. After 3 hours of stirring at room temperature, this was poured into 100 g of ice water, and the thus formed crystals were collected by filtration, washed with water-methanol and then dried under a reduced pressure to give 1.41 g of 2,4-dimethoxy-5-nitrobenzoic acid. The physicochemical properties were identical to those of the compound obtained by the former method.

後処理

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
  1. temperaturecooling
  2. filtrationthe thus formed crystals were collected by filtration
  3. washwashed with water-methanol
  4. customdried under a reduced pressure

出典と根拠

ORDレコード
ord-eae1be1159f04a688ca6cb2f406b11f5
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

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