HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1628511Generated: October 31, 2026
4-Chloro-2-methoxy-6-methyl-5-nitropyrimidine → 2-Methoxy-4,6-dimethyl-5-nitropyrimidine
https://huagongshe.com/reaction/1628511
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chloro-2-methoxy-6-methyl-5-nitropyrimidine | HCID 13080980 | — |
| Reactant | HCID 178477797 | HCID 178477797 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Methoxy-4,6-dimethyl-5-nitropyrimidine | HCID 68737303 | 93.4% |
Reaction Steps
Methylzinc chloride (2.0 M solution in tetrahydrofuran, 14.8 mL, 29.6 mmol) was added dropwise to a solution of 4-chloro-2-methoxy-6-methyl-5-nitropyrimidine (4.01 g, 19.7 mmol) and tetrakis(triphenyl phosphine)palladium (1.90 mmol) in tetrahydrofuran (60 mL), and the mixture was stirred at 50° C. for 50 minutes. The mixture was diluted with water, and extracted with ethyl acetate. The combined organic layer was washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel eluting with a 5-20% ethyl acetate/n-hexane gradient mixture. The filtrate was concentrated in vacuo to give the title compound as a pale yellow solid (3.37 g, 18.4 mmol, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08785460B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-2b625742042941e7bada9ce7bf46a03a |
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| Source note | uspto-grants-2014_07 |
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