Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 20490886 | HCID 20490886 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20317453 | HCID 20317453 | 92% |
Reaction Steps
150 g (0.5 mole) of 1-(2-[4"-chloro-4'-biphenylyl]-2-hydroxy-ethyl)-1,2,4-triazole were dissolved in 2 liters of chloroform and heated to the boil, while stirring. 90g (0.75 mole) of thionyl chloride were slowly added dropwise thereto. The reaction mixture was heated for 12 hours under reflux and after cooling, 1.5 liters of toluene were added. The hydrochloride of 1-(2-chloro-2-[4'(4"-chlorophenyl)-phenyl]-ethyl)-1,2,4-triazole, which thereupon precipitated, was filtered off and taken up in 2 liters of water. The free base was obtained by adding sodium bicarbonate, and was taken up in chloroform. After drying over sodium sulfate, the solvent was distilled off and the residue soldified to crystals. 148 g (92% of theory) of 1-(2-chloro-2-[4"-chloro-4'-biphenylyl]ethyl)-1,2,4-triazole of melting point 118° C. were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04102891 |
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| Source dataset | uspto-grants-1978_07 |
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| ORD ID | ord-7e46f44b38b942eba9fb5dc202712aa9 |
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| Source note | uspto-grants-1978_07 |
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