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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608764Generated: November 1, 2026

Dimethyl Sulfoxide → 2-(2,4-Dichlorophenyl)-2-[(1,2,4-triazol-1-yl)methyl]butyramide

https://huagongshe.com/reaction/1608764

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactantalpha-(2,4-dichlorophenyl)-alpha-ethyl-1H-1,2,4-triazole-1-propanenitrileHCID 54422114—
SolventEthyl AcetateHCID 8857—
Product2-(2,4-Dichlorophenyl)-2-[(1,2,4-triazol-1-yl)methyl]butyramideHCID 1995696479%

Reaction Conditions

Temperature91 °C

Reaction Steps

To a 1 liter flask was charged 206.5 g (0.7 mole) of alpha-(2,4-dichlorophenyl)-alpha-ethyl-1H-1,2,4-triazole-1-propanenitrile and 500 mL of dimethylsulfoxide and 200 mL of water. To the stirring solution was added 67.2 g (0.84 mole) of 50% sodium hydroxide. The reaction mixture was heated at 91° C. (steam bath) for 3 hours after which GLC indicated the starting material was consumed. The reaction was cooled to 30° C. then poured into water and extracted with ethyl acetate. After drying, the ethyl acetate was treated with charcoal and filtered through Celite®. Removal of the solvent gave a foamy oil which was stirred and diluted with ethyl acetate then triturated with hexane until cloudy. This mixture was cooled at 0° C. for about 1 hour after which a solid formed. The product was filtered and washed with ether and hexane then dried and provided 172 g (79% yield) of a white solid, Example 154 of Table 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05397768
Source datasetuspto-grants-1995_03
ORD IDord-338c2a1aa3434c87a2bacf37c0dc12ff
Source noteuspto-grants-1995_03