Methanol → HCID 20314720、化合物

HRID 2419151ノート

反応式

HRID 2419151 の反応式
[CH2:1]([N:3]([CH2:24][CH3:25])[C:4]1[CH:9]=[CH:8][C:7]([N:10]=[N:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([OH:20])=[O:19])=[C:14]([C:21]([OH:23])=[O:22])[CH:13]=2)=[CH:6][CH:5]=1)[CH3:2].[CH3:26]O>>[CH2:24]([N:3]([CH2:1][CH3:2])[C:4]1[CH:9]=[CH:8][C:7]([N:10]=[N:11][C:12]2[CH:17]=[CH:16][C:15]([C:18]([O:20][CH3:26])=[O:19])=[C:14]([C:21]([OH:23])=[O:22])[CH:13]=2)=[CH:6][CH:5]=1)[CH3:25]

参加物

3

反応物 2

HCID 887MethanolHCID 41695221,2-Benzenedicarboxylic acid, 4-[2-[4-(diethylamino)phenyl]diazenyl]-

生成物 1

HCID 20314720HCID 20314720、化合物

実験手順

1.6 Parts of the anhydride of N,N-diethyl-4(3,4-dicarboxyphenylazo)aniline is dissolved in 25 parts of methanol and the solution heated under reflux for 2 hours. The solution is then evaporated in vacuo to give N,N-diethyl-4(3-carboxy-4-carbomethoxyphenylazo)aniline which gives an orange solution in acetone with λmax 453.

後処理

  1. temperaturethe solution heated
  2. temperatureunder reflux for 2 hours
  3. customThe solution is then evaporated in vacuo

出典と根拠

ORDレコード
ord-18e32efae731466b8aa0cab829c43cdf
出典データセット
uspto-grants-1978_08
特許番号
USRE029724

反応ノート

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