HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180005Generated: November 2, 2026
(2-Methoxy-4,6-dimethylphenyl)boronic acid → HCID 22490043, compound
https://huagongshe.com/reaction/2180005
Participants
| Role | Name | HCID | Charge |
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| Reactant | (2-Methoxy-4,6-dimethylphenyl)boronic acid | HCID 21931520 | — |
| Reactant | HCID 22490069 | HCID 22490069 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Carbonate | HCID 10340 | — |
| Product | HCID 22490043 | HCID 22490043 | — |
Reaction Steps
A mixture of 2-chloro-4-methoxy-6-methylpyrimidin-5-ol (348 mg, 2.0 mmol), 2-methoxy-4,6-dimethylphenylboronic acid (540 mg, 3.0 mmol), tetrakis(triphenylphosphine)palladium (0) (115 mg, 5 mol %) in toluene (12 mL) and sodium carbonate (1M in water, 4 mL) is heated at 95° C. (oil bath temperature) in a pressure tube for 14 hours. The reaction is cooled to room temperature, diluted with ethyl acetate, washed with NaOH (2M) and then brine (2×50 mL). The solvents are dried (sodium sulfate) and removed under reduced pressure. Flash chromatography of the crude product (50% ethyl acetate in hexanes) yields 4-methoxy-2-(6-methoxy-2,4-dimethylphenyl)-6-methylpyrimidin-5-ol as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06887875B2 |
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| Source dataset | uspto-grants-2005_05 |
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| ORD ID | ord-d8fc84db2620473d8f40827898f1aadb |
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| Source note | uspto-grants-2005_05 |
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