HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 23463072, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 2-Chlorobenzoyl chloride | HCID 69110 | — |
| Reactant | 5-(2-Chlorophenyl)-1,3,4-thiadiazol-2-amine | HCID 554211 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 23463072 | HCID 23463072 | — |
Reaction Steps
10.5 g (0.05 mol) of 2-amino-5-(2-chlorophenyl)-1,3,4-thiadiazole, melting point 189,5° C. (prepared by reacting thiosemicarbazide with 2-chlorobenzoyl chloride) together with 10 g (0.05 mol) of bromoacetophenone are warmed to 120° C. in 100 ml of dimethylformamide for 3 hours and the mixture is then cooled and concentrated in a rotary evaporator. After digesting the residue with water, the digestion mixture is filtered and the residue is recrystallised from alcohol. A second fraction is obtained by concentrating the alcoholic mother liquor. A total yield of 12.5 g, corresponding to 80% of theory, of colourless crystals of melting point 126° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04265898 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-9f593c31b76e42e983b3e5a8b3cec8a0 |
| Source note | uspto-grants-1981_05 |