m-Chloroperbenzoic acid → HCID 22618454, compound

HRID 975529Notes

Reaction equation

HRID 975529 reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:17])([F:16])[F:15])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]([F:22])([F:21])[F:20])[C:3]=1[S:23][CH3:24].ClC1C=CC=C(C(OO)=[O:33])C=1>C(Cl)(Cl)Cl.ClCCl>[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([C:14]([F:15])([F:16])[F:17])=[CH:9][C:8]=2[Cl:18])[N:5]=[C:4]([C:19]([F:21])([F:20])[F:22])[C:3]=1[S:23]([CH3:24])=[O:33]

Participants

5

Procedure

A stirred solution of 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-methylthio-3-trifluoromethylpyrazole (1.0 g) in chloroform (40 ml) was treated with m-chloroperbenzoic acid (0.42 g), portionwise at room temperature. After stirring for 6 hours, the solution was diluted with dichloromethane and washed in turn with sodium sulphite solution, sodium hydroxide solution, and water. The solution was dried over anhydrous magnesium sulphate, and evaporated in vacuo to give a yellow oil. Purification by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm-2) eluting with dichloromethane-ethylacetate (4:1) gave 5-amino-1-(2,6-dichloro-4-trifluoromethylphenyl)-4-methylsulphinyl-3-trifluoromethylpyrazole in the form of a white solid, m.p. 142°-145° C. with decomposition.

Workup

  1. washwashed in turn with sodium sulphite solution, sodium hydroxide solution, and water
  2. dry with materialThe solution was dried over anhydrous magnesium sulphate
  3. customevaporated in vacuo
  4. customto give a yellow oil
  5. customPurification by chromatography on silica (Merck, 230-400 mesh, 0.7 kg cm-2)
  6. washeluting with dichloromethane-ethylacetate (4:1)

Sources & evidence

ORD record
ord-c47d78411f0f4e8e93ffe4d26d962c06
Source dataset
uspto-grants-1997_03
Patent number
US05608077

Reaction notes

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