HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrogen Bromide → 2-Bromo-2,4-dimethylpentan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | 2,4-Dimethyl-3-pentanone | HCID 11271 | — |
| Reactant | Bromine | HCID 24408 | — |
| Catalyst | Sodium Carbonate | HCID 10340 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-Bromo-2,4-dimethylpentan-3-one | HCID 222575 | 85.7% |
Reaction Steps
2,4-dimethyl-3-pentanone (330 g, 2.89M) in chloroform (800 ml) was cooled in an ice water bath to 10° C. and bromine (462 g, 2.89M) was added slowly over 3 hours. After the addition, a slow stream of nitrogen was introduced to the mixture and HBr gas was slowly evolved from the flask. The nitrogen was left bubbling over a weekend to remove all of the HBr produced and then sodium carbonate (5 g) was added. The reaction mixture was then filtered through Celite and the chloroform removed using a rotary evaporator. Distillation of the crude product using a 1′ (2.54 cm) vigreux gave essentially pure 2-bromo-2,4-dimethyl-3-pentanone (478 g, 2.47M) b.pt. 50-52° C./10 mb (1000 Nm−2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06559118B1 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-9814e21addcb449e80b9977d407c4ae5 |
| Source note | uspto-grants-2003_05 |