HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → 3-Butylpentane-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Acetylacetone | HCID 31261 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 3-Butylpentane-2,4-dione | HCID 73763 | 55.4% |
Reaction Steps
2,4-pentanedione (205.4 ml, 2.0 mol), acetone (100 ml), n-butyl bromide (54 ml, 0.5 mol), and potassium carbonate (34.55 g, 0.25 mol) were fed into a reaction vessel, air in the vessel was replaced with nitrogen, and reflux was carried out for 48 hours. The resultant solid was filtered out, and the solvent was distilled off by means of an evaporator. After that, unreacted 2,4-pentanedione was distilled off under reduced pressure by means of a diaphragm. Then, the remainder was distilled in a vacuum to yield 3-n-butyl 2,4-pentanedione (43.25 g, 55% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07928221B2 |
| Source dataset | uspto-grants-2011_04 |
| ORD ID | ord-51bb00867c1e4642bb1cfb8d12896db8 |
| Source note | uspto-grants-2011_04 |