Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-[2-Chloro-2-(2,4-dichlorophenyl)ethyl]-1H-1,2,4-triazole | HCID 13488616 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20285387 | HCID 20285387 | — |
Reaction Steps
12.55 parts by weight of butylmercaptan is dripped into a suspension of 3.33 parts by weight of sodium hydride in 180 parts by weight of tetrahydrofuran. A solution of 27.5 parts by weight of 1-[2-chloro-2-(2,4-dichlorophenyl)-ethyl]-1,2,4-triazole in 50 parts of tetrahydrofuran is then dripped in and the mixture is stirred for 3 days at room temperature. The mixture is concentrated, stirred with water, and extracted with dichloromethane. The resulting dichloromethane solution is dried and evaporated. There is obtained 29.5 parts of crude 1-[2-n-butylmercapto-2-(2,4-dichlorophenyl)-ethyl]-1,2,4-triazole, which is dissolved in ethyl acetate. When hydrogen chloride is passed into the ethyl acetate solution, 25.9 parts of 1-[2-n-butylmercapto-2-(2,4-dichlorophenyl)-ethyl]-1,2,4-triazole hydrochloride, m.p. 143° C., precipitates out.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04256754 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-01a85a6c040c4d478281a98218ad40d8 |
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| Source note | uspto-grants-1981_03 |
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