HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Bromide → HCID 15136695, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 12563150 | HCID 12563150 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 15136695 | HCID 15136695 | 52% |
Reaction Steps
4,4-dimethyl-3-pyrazolidinone [1.42 g] and benzyl bromide [1.78 mL] and NaHCO3 [1.26 g] were combined in 5 mL ethanol. The mixture was heated at reflux for 30 minutes. The reaction mixture was cooled to room temperature, diluted with diethyl ether (50 mL), dried with MgSO4, filtered and evaporated. The resulting oil was chromatographed on silica gel to yield 1.22 g (52%) of 1-Benzyl-4,4-dimethyl-3-pyrazolidinone as a light oil. 1H NMR: 7.6-7.2 (5H, m), 3.8-3.4 (4H, m), 1.2 (6H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05196546 |
| Source dataset | uspto-grants-1993_03 |
| ORD ID | ord-5f71700c202a4424bdcec368a767730b |
| Source note | uspto-grants-1993_03 |