HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387723Generated: November 1, 2026
Chloroform → 5-Methoxy-2,4-dimethylpyrimidine
https://huagongshe.com/reaction/2387723
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroform | HCID 6212 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 2,4-Dichloro-5-methoxypyrimidine | HCID 601401 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 5-Methoxy-2,4-dimethylpyrimidine | HCID 67283705 | — |
Reaction Steps
2,4-Dichloro-5-methoxypyrimidine (5.3 g) was dissolved in THF (51.3 ml), and tetrakis(triphenylphosphine)palladium (1.71 g) and trimethylaluminum (2.0 M: 51.8 ml) were then added to the solution. The temperature of the obtained mixture was heated to 75° C., and the obtained mixture was then stirred overnight. Thereafter, 1 equivalent of trimethyl aluminum was added to the reaction solution, and the obtained mixture was then stirred for 6 hours. Thereafter, saturated ammonium chloride aqueous solution was added dropwise to the reaction solution under cooling on ice, and liquid separation and extraction were carried out with chloroform. The organic layer was dried over magnesium sulfate, and the solvent was then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (n-heptane:ethyl acetate to ethyl acetate), so as to obtain the title compound (4.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08268848B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-453f65ddecc94a53814caff9aa8883c3 |
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| Source note | uspto-grants-2012_09 |
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