Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13268168 | HCID 13268168 | — |
| Reactant | 2-(4-Chlorophenyl)-4-(2-thienyl)butyronitrile | HCID 19738026 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 19738052 | HCID 19738052 | — |
Reaction Steps
To a flask under a nitrogen atmosphere was added, with stirring, 1.5 g. (0.036 mole) of 60% sodium hydride, washed twice with hexane to remove the original mineral oil, in 30 ml. of dry DMF. To this slurry at room temperature was added 3.36 g. (12.8 mmoles) of 2-(4-chlorophenyl)-4-(2-thienyl)butyronitrile in 30 ml. of DMF over 10 minutes. After stirring for 30 minutes, 2.15 g. (14.08 mmoles) of 1-(chloromethyl)-1,2,4-triazole hydrochloride was added in two portions and stirred for another 60 minutes. Water, 20 ml., was then added followed by 100 ml. of ether. The ether layer was washed twice with 50 ml. portions of water and the water washes further extracted with 50 ml. of ether. The combined ether extracts were chromatographed on 50 g. of silica gel. The product was eluted with ethyl acetate yielding 1.17 g. of product as a thick brown oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05240925 |
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| Source dataset | uspto-grants-1993_08 |
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| ORD ID | ord-69469907670e4ad4979462923c915ff6 |
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| Source note | uspto-grants-1993_08 |
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