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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethyl Sulfoxide | HCID 679 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | alpha-(2,4-dichlorophenyl)-alpha-ethyl-1H-1,2,4-triazole-1-propanenitrile | HCID 54422114 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(2,4-Dichlorophenyl)-2-[(1,2,4-triazol-1-yl)methyl]butyramide | HCID 19956964 | 79% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05397768 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-338c2a1aa3434c87a2bacf37c0dc12ff |
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| Source note | uspto-grants-1995_03 |
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