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Water → 4-(p-Toluenesulfonylmethyl)-2,6-dihydroxymethyl-s-triazine

HRID 1421677
ノート
印刷プレビュー

反応式

HRID 1421677 の反応式
O[CH2:2][C:3]1[N:8]=[C:7]([CH2:9][OH:10])[N:6]=[C:5]([CH2:11][OH:12])[N:4]=1.N1C=CC=CC=1.[C:19]1([CH3:29])[CH:24]=[CH:23][C:22]([S:25](Cl)(=[O:27])=[O:26])=[CH:21][CH:20]=1.O>C(Cl)Cl>[C:19]1([CH3:29])[CH:24]=[CH:23][C:22]([S:25]([CH2:2][C:3]2[N:8]=[C:7]([CH2:9][OH:10])[N:6]=[C:5]([CH2:11][OH:12])[N:4]=2)(=[O:27])=[O:26])=[CH:21][CH:20]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 1049PyridineHCID 73974-Toluenesulfonyl chlorideHCID 223236642,4,6-Trihydroxymethyl-s-triazine

生成物 1

HCID 223236944-(p-Toluenesulfonylmethyl)-2,6-dihydroxymethyl-s-triazine

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒2 回

実験手順

2,4,6-Trihydroxymethyl-s-triazine (1 eq.) is dissolved in an excess of pyridine. p-Toluenesulfonylchloride (0.9 eq.) in CH2Cl2 is added and the reaction mixture is stirred overnight. The solvent volume is reduced to a slurry to which water and dichloromethane are added and the resulting mixture is extracted with CH2Cl2. The combined CH2Cl2 layers are dried (MgSO4) and concentrated to an oil. The oil is purified by silica gel flash column chromatography to give the title compound.

後処理

  1. additionare added
  2. extractionthe resulting mixture is extracted with CH2Cl2
  3. dry with materialThe combined CH2Cl2 layers are dried (MgSO4)
  4. concentrationconcentrated to an oil
  5. customThe oil is purified by silica gel flash column chromatography

出典と根拠

ORDレコード
ord-a096e5a92b304f6b8ec51664f6e477f4
出典データセット
uspto-grants-2000_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06077954

反応ノート

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