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Phosphorus oxychloride → 5-Acetylamino-2-chloro-4-(4-chlorosulfonyl-2-methylsulfonylphenylazo)phenol

HRID 1252025
ノート
印刷プレビュー

反応式

HRID 1252025 の反応式
[CH3:1][S:2]([C:5]1[CH:6]=[C:7]([S:25]([O-:28])(=O)=[O:26])[CH:8]=[CH:9][C:10]=1[N:11]=[N:12][C:13]1[CH:18]=[C:17]([Cl:19])[C:16]([OH:20])=[CH:15][C:14]=1[NH:21][C:22](=[O:24])[CH3:23])(=[O:4])=[O:3].[Ca+2].CS(C1C=C(S([O-])(=O)=O)C=CC=1N=NC1C=C([Cl:48])C(O)=CC=1NC(=O)C)(=O)=O.CC(N(C)C)=O.P(Cl)(Cl)(Cl)=O>C(#N)C>[C:22]([NH:21][C:14]1[C:13]([N:12]=[N:11][C:10]2[CH:9]=[CH:8][C:7]([S:25]([Cl:48])(=[O:28])=[O:26])=[CH:6][C:5]=2[S:2]([CH3:1])(=[O:4])=[O:3])=[CH:18][C:17]([Cl:19])=[C:16]([OH:20])[CH:15]=1)(=[O:24])[CH3:23]
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 3

HCID 24813Phosphorus oxychlorideHCID 31374DimethylacetamideHCID 136342787Calcium 3-methylsulfonyl-4-(2-acetylamino-5-chloro-4-hydroxyphenylazo)phenylsulfonate

生成物 1

HCID 1355831435-Acetylamino-2-chloro-4-(4-chlorosulfonyl-2-methylsulfonylphenylazo)phenol

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

実験手順

To a suspension of 18 g of calcium 3-methylsulfonyl-4-(2-acetylamino-5-chloro-4-hydroxyphenylazo)phenylsulfonate, 25 ml of dimethylacetamide, and 54 ml of acetonitrile was added dropwise to 18 ml of phosphorus oxychloride at room temperature with stirring. After completion of the addition, the reaction was allowed to proceed at 60° C. for 3 hours, and the reaction mixture was cooled to room temperature and then poured in 1 l of ice water. The mixture was stirred at a temperature of 10° C. or less for 1 hour and the resulting crystalline precipitate was collected by filtration, washed with water and air-dried.

後処理

  1. additionAfter completion of the addition
  2. stirringThe mixture was stirred at a temperature of 10° C. or less for 1 hour
  3. filtrationthe resulting crystalline precipitate was collected by filtration
  4. washwashed with water
  5. customair-dried

出典と根拠

ORDレコード
ord-99c79e2056094d54863bae3180c3fe18
出典データセット
uspto-grants-1988_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04741997

反応ノート

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