HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Pyrrolidone → Ethyl 4-(2-bromopropanoyl)benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Pyrrolidone | HCID 12025 | — |
| Reactant | Ethyl 4-propanoylbenzoate | HCID 24727466 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-(2-bromopropanoyl)benzoate | HCID 71424477 | — |
Reaction Steps
Ethyl 4-propionylbenzoate (2.0 mmol), pyrrolidinone hydrotribromide (2.1 mmol) and 2-pyrrolidinone (2.2 mmol) were heated in THF (20 mL) at 50 C for 2.5 h. The mixture was cooled, filtered, concentrated under vacuum and the residual oil partitioned between H2O and MTBE. The aqueous layer was extracted with MTBE, and the combined organic layers were washed with saturated aqueous sodium metabisulfite solution, H2O, brine, dried over MgSO4 and the solvent removed under vacuum. The residue was purified by flash column chromatography (9:1 IHexane: MTBE) to afford ethyl-4(2′-bromopropionyl)benzoate as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915300B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-9f111510cfe34fd8b557726ce23a9836 |
| Source note | uspto-grants-2011_03 |