Dimethyl Sulfate → HCID 12877073, compound

HRID 1164230Notes

Reaction equation

HRID 1164230 reaction equation
[CH3:1][C:2]1[N:3]([C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-:16])=[O:15])=[CH:10][CH:9]=2)[C:4](=[O:7])[NH:5][N:6]=1.[H-].[Na+].S(OC)(O[CH3:23])(=O)=O>CS(C)=O>[CH3:23][N:5]1[C:4](=[O:7])[N:3]([C:8]2[CH:9]=[CH:10][C:11]([N+:14]([O-:16])=[O:15])=[CH:12][CH:13]=2)[C:2]([CH3:1])=[N:6]1

Participants

5

Procedure

To a stirred solution of 13.5 parts of 2,4-dihydro-5-methyl-4-(4-nitrophenyl)-3H-1,2,4-triazol-3-one in 100 parts of dimethyl sulfoxide are added 2 parts of sodium hydride dispersion 78% and the whole is stirred till foaming has ceased. Then there are added dropwise 8.1 parts of dimethyl sulfate. Upon completion, stirring is continued for 3 hours at room temperature. The reaction mixture is poured onto water and the product is extracted three times with trichloromethane. The combined extracts are washed with water, dried, filtered and evaporated. The residue is crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product is filtered off and recrystallized from 4-methyl-2-pentanone, yielding 6.3 parts of 2,4-dihydro-2,5-dimethyl-4-(4-nitrophenyl)-3H-1,2,4-triazol-3-one; mp. 153.2° C.

Workup

  1. stirringUpon completion, stirring
  2. additionThe reaction mixture is poured onto water
  3. extractionthe product is extracted three times with trichloromethane
  4. washThe combined extracts are washed with water
  5. customdried
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue is crystallized from a mixture of 2-propanol and 2,2'-oxybispropane
  9. filtrationThe product is filtered off
  10. customrecrystallized from 4-methyl-2-pentanone

Sources & evidence

ORD record
ord-9f33e9a2c149463a9bb0e09e967a6dd6
Source dataset
uspto-grants-1983_01
Patent number
US04368200

Reaction notes

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