HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → Ethyl alpha-benzylacetoacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Ethyl Acetoacetate | HCID 8868 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl alpha-benzylacetoacetate | HCID 246929 | 74% |
Reaction Steps
0.1 Mol of ethyl acetoacetate, 0.1 mol of K2CO3, 0.1 mol of benzyl bromide, 0.01 mmol of PEG-400 (polyethylene glycol 400) and 100 ml of benzene were stirred at 75° C. for 7 hours. After cooling, 20 ml of saturated solution of NH4Cl was added to dissolve solid, and product was extracted with ethyl acetate. After removing the solvent, the residue was distilled under reduced pressure, and a cut fraction was collected at 116-118° C./20 Pa. Yield 74%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07351778B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-e2405c4aecdd42af8025950385979ec4 |
| Source note | uspto-grants-2008_04 |