HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromomethyl 4-methoxyphenyl ketone → 3-(p-Methoxy-phenacylmercapto)-4-n-butyl-1,2,4-triazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromomethyl 4-methoxyphenyl ketone | HCID 4965 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 178448642 | HCID 178448642 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(p-Methoxy-phenacylmercapto)-4-n-butyl-1,2,4-triazole | HCID 12888464 | — |
Reaction Steps
To a solution of 3-mercapto-4-n-butyl-1,2,4-triazole (10 g. or 0.063 mole) and sodium hydroxide (2.55 g. or 0.0637 mole) in 200 ml. of methanol was added α-bromo-p-methoxyacetophenone (15.3 g. or 0.067 mole). The reaction mixture was heated at reflux for 16 hours and the solvent removed in vacuum to leave a solid residue. The solid was washed with water and recrystallized from benzene-hexane to give 3-(p-methoxy-phenacylmercapto)-4-n-butyl-1,2,4-triazole melting at 79°-82° C. The structure was confirmed by its infrared and nuclear magnetic spectra.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04120864 |
| Source dataset | uspto-grants-1978_10 |
| ORD ID | ord-e9809cf5a2f34f45aba3e25b02b33eb1 |
| Source note | uspto-grants-1978_10 |