HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373161Generated: October 30, 2026
1H-1,2,4-Triazole → HCID 19811975, compound
https://huagongshe.com/reaction/373161
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 19811974 | HCID 19811974 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19811975 | HCID 19811975 | 46.5% |
Reaction Steps
12 g (174 mmol) of 1,2,4-triazole and 17 g (123 mmol) of potassium carbonate are initially introduced into 30 ml of absolute dimethylformamide under a nitrogen atmosphere and the mixture is heated to 80° C. At this temperature, a solution of 16.7 g (55.5 mmol) of 1-chloro-3-(2-chlorophenyl)-2-(1-methyl-cyclohex-1-yl)-propan-2-ol in 20 ml of absolute dimethylformamide is added dropwise with stirring. The reaction mixture is then stirred at 80° C. for a further 8 hours. The precipitate is filtered off with suction, and the filtrate is concentrated by stripping off the diluent under reduced pressure. The residue is taken up in ethyl acetate, washed with water and, after drying over sodium sulphate, the solvent is stripped off under reduced pressure. The product which remains is chromatographed through a silica gel column using dichloromethane/ethanol=99:1 as the eluent. 8.6 g (46.5% of theory) of 1-(2-chlorophenyl)-2-(1-methyl-cyclohex-1-yl)-3 -(1,2,4-triazol-1-yl)-propan-2-ol are obtained in this manner in the form of a solid substance of melting point 105° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05162355 |
|---|
| Source dataset | uspto-grants-1992_11 |
|---|
| ORD ID | ord-718bebf8961545c4b472062adaebb075 |
|---|
| Source note | uspto-grants-1992_11 |
|---|