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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387723Generated: November 1, 2026

Chloroform → 5-Methoxy-2,4-dimethylpyrimidine

https://huagongshe.com/reaction/2387723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantTetrahydrofuranHCID 8028—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,4-Dichloro-5-methoxypyrimidineHCID 601401—
ReactantTrimethylaluminumHCID 16682925—
CatalystHCID 178418397HCID 178418397—
Product5-Methoxy-2,4-dimethylpyrimidineHCID 67283705—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268848B2
Source datasetuspto-grants-2012_09
ORD IDord-453f65ddecc94a53814caff9aa8883c3
Source noteuspto-grants-2012_09