HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → 2-Amino-4-phenylthiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Amino-4-phenylthiazole | HCID 40302 | 82.4% |
Reaction Steps
A mixture of 2 g of phenacylbromide and 0.76 g of thiourea in 50 mL ethanol was refluxed overnight. After solvent evaporation, the residue was redissolved in 50 mL DCM and treated by 50 mL of a 2% sodium carbonate solution in water. The organic layer was dried and evaporated to yield 1.45 g (82%) of 4-phenyl-2-thiazolamine (intermediate p. Mass spectral data: m/z=177 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07763641B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-8ab7c3e46ae640af8946d02a5ab527df |
| Source note | uspto-grants-2010_07 |