HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 572636Generated: November 1, 2026
Sodium Carbonate → Methyl 6-bromo-2-methylpyrimidine-4-carboxylate
https://huagongshe.com/reaction/572636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | HCID 178498594 | HCID 178498594 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 6-bromo-2-methylpyrimidine-4-carboxylate | HCID 86675899 | — |
Reaction Steps
POBr3 (6.65 g, 23.2 mmol, Spectrochem) was added to a stirred solution of methyl 6-hydroxy-2-methylpyrimidine-4-carboxylate (5.0 g, 29.7 mmol, Preparation #2) in DMF (100 mL) at about 90° C. The reaction mixture was heated at the same temperature for about another 10 min and poured into ice water (500 mL). The solution was neutralized with 10% aqueous sodium carbonate solution (pH 7). This solution was extracted with EtOAc (3×200 mL). The combined organic layer was washed with water (2×100 mL) and brine solution (2×150 mL), and dried over sodium sulphate and concentrated in vacuum. The crude material was purified by silica gel chromatography using 15 to 25% of EtOAc in hexane as the eluent. Relevant fractions containing the required compound were combined and evaporated to dryness under reduced pressure to afford methyl 6-bromo-2-methylpyrimidine-4-carboxylate as an off white solid 5.2 g (75.7%). 1H NMR (400 MHz, DMSO) δ: 8.02 (s, 1H), 4.03 (s, 3H), 2.83 (s, 3H); MS m/z: 231 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09029409B2 |
|---|
| Source dataset | uspto-grants-2015_05 |
|---|
| ORD ID | ord-dd8679db4be94093bccee52f06029765 |
|---|
| Source note | uspto-grants-2015_05 |
|---|