HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1038118Generated: November 4, 2026
Ethanol → 2-(4-Bromo-2,3-difluoro-phenyl)-pyrimidine
https://huagongshe.com/reaction/1038118
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Bromopyrimidine | HCID 78345 | — |
| Reactant | 4-Bromo-2,3-difluorobenzeneboronic acid | HCID 2773292 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(4-Bromo-2,3-difluoro-phenyl)-pyrimidine | HCID 57685931 | — |
Reaction Steps
A mixture of 2-bromopyrimidine (2.0 g, 12.7 mmol), 4-bromo-2,3-difluorobenzeneboronic acid (1.0 g, 4.22 mmol), potassium carbonate (2.93 g, 21.1 mmol) in a mixture of toluene (30 ml)/ethanol (30 ml)/water (15 ml) were purged with nitrogen for 15 min. Tetrakis(triphenylphosphine)palladium(0) (488 mg, 0.42 mmol) was added and the mixture was stirred at 90° C. in a sealed-tube for overnight. The mixture was cooled to r.t. and was diluted with water and ethyl acetate. Layers were separated. The separated organic layer was dried (MgSO4), filtered and solvents were removed in vacuum. Column purification [Hexanes-Ethyl acetate, 2:1 (v/v)] gave bromide 3AC (0.97 g, 85%) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08546404B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-5414e2b09a2c40629eb0f0a956f0615b |
|---|
| Source note | uspto-grants-2013_10 |
|---|