m-Chloroperbenzoic acid → 3-(Methanesulfinyl)-4-methyl-5-(naphthalen-2-yl)-4H-1,2,4-triazole

HRID 257164Notes

Reaction equation

HRID 257164 reaction equation
[CH3:1][N:2]1[C:6]([S:7][CH3:8])=[N:5][N:4]=[C:3]1[C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=1.ClC1C=C(C=CC=1)C(OO)=[O:24]>C(Cl)Cl>[CH3:1][N:2]1[C:6]([S:7]([CH3:8])=[O:24])=[N:5][N:4]=[C:3]1[C:9]1[CH:18]=[CH:17][C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:10]=1

Participants

4

Reactant 2

HCID 70297m-Chloroperbenzoic acidHCID 30879994H-1,2,4-Triazole, 4-methyl-3-(methylthio)-5-(2-naphthalenyl)-

Product 1

HCID 30880023-(Methanesulfinyl)-4-methyl-5-(naphthalen-2-yl)-4H-1,2,4-triazole

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

To a stirred, 0° C., solution of 4-methyl-5-methylthio-3-(2-naphthyl)-4H-1,2,4-triazole (4.00 g, 1.57×10-2 mole) and CH2Cl2 (110 ml) was added portionwise m-chloroperoxybenzoic acid (3.38 g, 1.57×10-2 mole). overnight at room temperature the reaction was diluted with CH2 l2 (200 ml), washed two times with saturated aqueous NaHCO3 and one time with saturated aqueous NaCl, and dried over anhydrous Na2SO4. The drying agent was removed by filtration and the filtrate was evaporated at reduced pressure leaving an off-white solid which was purified by flash chromatography (4% CH3OH/CH2Cl2). Crystallization from toluene afforded small colorless plates: Mp 224°-226° C.

Workup

  1. additionovernight at room temperature the reaction was diluted with CH2 l2 (200 ml)
  2. washwashed two times with saturated aqueous NaHCO3 and one time with saturated aqueous NaCl
  3. dry with materialdried over anhydrous Na2SO4
  4. customThe drying agent was removed by filtration
  5. customthe filtrate was evaporated at reduced pressure
  6. customleaving an off-white solid which
  7. customwas purified by flash chromatography (4% CH3OH/CH2Cl2)
  8. customCrystallization from toluene afforded small colorless plates

Sources & evidence

ORD record
ord-a740b401cb5f4b55883a12a95ccbd864
Source dataset
uspto-grants-1993_11
Patent number
US05260450

Reaction notes

Loading…