HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzaldehyde → 3-(4-Bromophenyl)-1-phenyl-2-propen-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzaldehyde | HCID 240 | — |
| Reactant | Acetophenone | HCID 7410 | — |
| Reactant | p-Bromoacetophenone | HCID 7466 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-(4-Bromophenyl)-1-phenyl-2-propen-1-one | HCID 102159 | 93% |
Reaction Steps
Sodium hydroxide (1.88 g, 47 mmol) and 4-bromoacetophenone (7.47 g, 37.5 mmol) were dissolved in water (15 mL) and ethanol (50 mL). Benzaldehyde (4.00 g, 37.5 mmol) dissolved in ethanol (20 mL) was added dropwise to the acetophenone solution. A slurry quickly formed, which was allowed to stir overnight. The slurry was filtered, was with water until the filtrate was neutral to pH paper, and dried at 100° C. for 12 hours. A light tan solid was obtained (10.0 g, 93% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067702B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-7e09a1cac851415bbf0883d7c87b03de |
| Source note | uspto-grants-2006_06 |