Potassium Carbonate → HCID 20323003、化合物

HRID 839485

反応式

HRID 839485 の反応式
Cl[C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[C:9](Cl)[CH:10]=[CH:11][C:12]=3Cl)[C:7](=[O:19])[C:6]=2[C:5](Cl)=[CH:4][CH:3]=1.[SH:21][C:22]1[S:23][C:24]2[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=2[N:26]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[S:23]1[C:24]2[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=2[N:26]=[C:22]1[S:21][C:2]1[C:15]2[C:14](=[O:16])[C:13]3[C:8](=[C:9]([S:21][C:22]4[S:23][C:24]5[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=5[N:26]=4)[CH:10]=[CH:11][C:12]=3[S:21][C:22]3[S:23][C:24]4[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=4[N:26]=3)[C:7](=[O:19])[C:6]=2[C:5]([S:21][C:22]2[S:23][C:24]3[CH:30]=[CH:29][CH:28]=[CH:27][C:25]=3[N:26]=2)=[CH:4][CH:3]=1

参加物

5

実験手順

The dyestuff used can be prepared as follows: 15 g of 1,4,5,8-tetrachloro-anthraquinone, 75 g of dimethylformamide, 35 g of 2-mercaptobenzthiazole and 30 g of potassium carbonate are heated to 125°-130° C for about 3 hours. After cooling, the dyestuff which has precipitated in attractive red prisms is filtered off and washed with methanol and water. After drying, 34 g of 1,4,5,8-tetra-(2-benzthiazolyl-thio)-anthraquinone = 90% of theory are obtained.

後処理

  1. customThe dyestuff used can be prepared
  2. temperatureAfter cooling
  3. customthe dyestuff which has precipitated in attractive red prisms
  4. filtrationis filtered off
  5. washwashed with methanol and water
  6. customAfter drying

出典と根拠

ORDレコード
ord-fffa3eaafbea410f8682c6dc41685fef
出典データセット
uspto-grants-1978_06
特許番号
US04096111

関連ノート

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