HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 895892Generated: October 30, 2026
Benzyl Bromide → 1-Benzyl-3-bromo-5-chloro-2-pyridone
https://huagongshe.com/reaction/895892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl Bromide | HCID 7498 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Bromo-5-chloropyridin-2-ol | HCID 2726791 | — |
| Catalyst | Tetrabutylammonium Chloride | HCID 70681 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-Benzyl-3-bromo-5-chloro-2-pyridone | HCID 22382054 | 31.1% |
Reaction Steps
A mixture of 3-bromo-5-chloro-1H-2-pyridone (950 mg, 4.56 mmol), freshly ground potassium carbonate (1.26 g, 9.1 mmol) and tetrabutyl ammonium chloride (100 mg) in was stirred mechanically without solvent for 30 min and benzyl bromide (0.56 mL, 4.7 mmol) was added. The mixture was stirred at room temperature for 72 hr. The mixture was diluted with ethyl acetate and filtered, washing the solids with ethyl acetate. The filtrate was evaporated to dryness and the residue was triturated with several portions of hexane. The residue was chromatographed over 90 g of silica gel eluting with 3:1 hexane:ethyl acetate followed by 100% ethyl acetate to give 1-benzyl-3-bromo-5-chloro-2-pyridone (423 mg, 31%), mp 108-110° C. LR(+)LSIMS: m/z 595 (2M+H, 2 Cl, 2 Br), 298 (M+H, 1 Cl, 1 Br).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06916933B2 |
|---|
| Source dataset | uspto-grants-2005_07 |
|---|
| ORD ID | ord-18ca42917f424cbcbece01bd7afc719b |
|---|
| Source note | uspto-grants-2005_07 |
|---|