Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | 2-Benzyl-1,3-dioxolane | HCID 7562 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Product | 1-Methyl-4-phenyl-1H-pyrazole | HCID 13692442 | — |
Reaction Steps
32.8 g (0.20 mol) of 2-benzyl-1,3-dioxolane are introduced, at a temperature of between 50° C. and 65° C., into a reactor containing 57.6 g (0.45 mol) of N,N-dimethylchloromethyliminium chloride in solution in 150 ml of chloroform and the solution is then heated for 1 h to 65° C. The chloroform is removed under reduced pressure and 11.5 g (0.25 mol) of monomethylhydrazine in aqueous solution at a concentration of 30% are then introduced at 50° C. The solution is heated for 2 h at 70° C. It is cooled to 20° C. and then neutralised to pH =8 with an aqueous 30% sodium hydroxide solution. 10 ml of water are then added and the required product is then extracted with 2 15-ml portions of methylene chloride. The extraction solvent is removed. A crude product is thus obtained, which was purified by recrystallisation from isopropyl ether. The purified product, 1-methyl-4-phenylpyrazole, identified by 1H NMR and mass spectrometry, has a melting point of 103.6° C. The yield of 1-methyl-4-phenylpyrazole formed, determined by quantitative analysis of the crude product, is 46%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05191087 |
|---|
| Source dataset | uspto-grants-1993_03 |
|---|
| ORD ID | ord-4e38c5f0c073492ca83c799ef666edb6 |
|---|
| Source note | uspto-grants-1993_03 |
|---|