HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phenacyl bromide → HCID 178512605, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | HCID 178513045 | HCID 178513045 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 178512605 | HCID 178512605 | 87% |
Reaction Steps
A mixture of amidinothiourea (2.0 g, 16.9 mmol), 2-bromoacetophenone (3.4 g, 16.9 mmol) was heated at reflux in acetone (12 mL) for 4 h. The mixture was cooled to room temperature and removed half of the solvent. The precipitate was filtered, washed with acetone, and dried to give N-(4-phenyl-1,3-thiazol-2-yl)guanidine (3.2 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07462723B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-127842b416614ecf891fb49d0f3337d0 |
| Source note | uspto-grants-2008_12 |