HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → 4-(2-Chloro-5-fluorophenyl)-3-buten-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chloro-5-Fluorobenzaldehyde | HCID 2779184 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-Chloro-5-fluorophenyl)-3-buten-2-one | HCID 53922918 | — |
Reaction Steps
In water (55 ml) was dissolved sodium hydroxide (0.78 g), and to the mixture was added acetone (55 ml), and then added dropwise a solution of 2-chloro-5-fluorobenzaldehyde (2.8 g) in acetone (10 ml). The reaction solution was stirred at room temperature for 2 hours, and acetone was evaporated under reduced pressure. The residue was extracted with ethyl acetate, and the organic layer was washed with water and saturated brine, and concentrated under reduced pressure to give 4-(2-chloro-5-fluorophenyl)-3-buten-2-one (0.24 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06350749B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-6fd708a4a92d4e519a67e8b4383bce2f |
| Source note | uspto-grants-2002_02 |