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

HRID 1533476Notes

Reaction equation

HRID 1533476 reaction equation
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>ClCCl>[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

Participants

6

Procedure

2,4,6-Trihydroxymethyl-s-triazine (1 eq.) is dissolved in an excess of pyridine. p-Toluenesulfonylchloride (0.6 eq.) in CH2Cl2is 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.

Workup

  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

Sources & evidence

ORD record
ord-d438274873674ca295c152f23fa33c1b
Source dataset
uspto-grants-2001_03
Patent number
US06207826B1

Reaction notes

Loading…