Hydrogen Peroxide → HCID 20533546, compound
Reaction equation
[SH:1][C:2]1[N:3]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:4]([CH2:7][OH:8])=[N:5][N:6]=1.[OH-:15].[Na+].Br[CH2:18]C.OO>>[CH3:18][S:1]([C:2]1[N:3]([C:9]2[CH:10]=[CH:11][CH:12]=[CH:13][CH:14]=2)[C:4]([CH2:7][OH:8])=[N:5][N:6]=1)=[O:15]Participants
5
Procedure
Refer to Chart F. One equivalent of 5-mercapto-4-phenyl-4H-1,2,4-triazole-3-methanol (Formula XXIII of Chart B, R24 is hydroxymethyl, R5 is phenyl, n is zero) is prepared according to Chart B. One equivalent of this compound is treated with sodium hydroxide and bromoethane. This product is then oxidized with aqueous hydrogen peroxide to yield 5-methylsulfinyl-4-phenyl-4H-1,2,4-triazole-3-methanol. This product is further oxidized by treating it with m-chlorobenzoic acid at 25° C. for 24 hrs to yield the titled product.
Workup
- customis prepared
Sources & evidence
- ORD record
- ord-165c951f35754cbd8a7d60f123585f4b
- Source dataset
- uspto-grants-1982_07
- Patent number
- US04338453
Reaction notes
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