6-Amino-1,3-naphthalenedisulfonic acid → 6,6'-[5-Nitro-1,3-phenylenebis(carbonylimino)]bis[1,3-naphthalenedisulfonic acid] tetrasodium salt

HRID 65905

反応式

HRID 65905 の反応式
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[C:8]([S:12]([OH:15])(=[O:14])=[O:13])=[CH:7][C:6]([S:16]([OH:19])(=[O:18])=[O:17])=[CH:5]2.[C:20]([O-])(=O)[CH3:21].[Na+:24].[N+:25]([C:28]1[CH:29]=[C:30]([C:37](Cl)=[O:38])[CH:31]=[C:32]([C:34](Cl)=[O:35])[CH:33]=1)([O-:27])=[O:26]>O>[Na+:24].[Na+:24].[Na+:24].[Na+:24].[N+:25]([C:28]1[CH:29]=[C:30]([C:37]([NH:1][C:2]2[CH:3]=[C:4]3[C:9](=[CH:20][CH:21]=2)[C:8]([S:12]([O-:15])(=[O:14])=[O:13])=[CH:7][C:6]([S:16]([O-:19])(=[O:18])=[O:17])=[CH:5]3)=[O:38])[CH:31]=[C:32]([C:34]([NH:1][C:2]2[CH:3]=[C:4]3[C:9](=[CH:10][CH:11]=2)[C:8]([S:12]([O-:15])(=[O:14])=[O:13])=[CH:7][C:6]([S:16]([O-:19])(=[O:18])=[O:17])=[CH:5]3)=[O:35])[CH:33]=1)([O-:27])=[O:26]

参加物

5

実験手順

An 18.18 g portion of 6-amino-1,3-naphthalenedisulfonic acid is suspended in 200 ml of water and the pH is adjusted to 7.0 giving a solution. A 5.6 g portion of sodium acetate is dissolved in this solution and 8.18 g of 5-nitro-1,3-benzenedicarbonyl dichloride is added. The mixture is stirred for one hour, filtered and the filtrate is treated with activated carbon. The filtrate is reduced to a low volume on a rotary evaporator producing crystals. The crystals are recrystallized from water giving 6,6'-[5-nitro-1,3-phenylenebis(carbonylimino)]bis[1,3-naphthalenedisulfonic acid] tetrasodium salt.

後処理

  1. additionis added
  2. filtrationfiltered
  3. additionthe filtrate is treated with activated carbon
  4. customThe filtrate is reduced to a low volume on a rotary evaporator
  5. customproducing crystals
  6. customThe crystals are recrystallized from water

出典と根拠

ORDレコード
ord-cf631a3b80ae4c49b0a14aa93c206573
出典データセット
uspto-grants-1978_12
特許番号
US04129591

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