HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170803Generated: October 29, 2026
Potassium Phosphate, Tribasic → 2-[2-(4-Chloro-phenyl)-5-methyl-pyrimidin-4-yl]-cyclopentane-1,3-dione
https://huagongshe.com/reaction/2170803
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1,3-Cyclopentanedione | HCID 77466 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | HCID 178430308 | HCID 178430308 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-[2-(4-Chloro-phenyl)-5-methyl-pyrimidin-4-yl]-cyclopentane-1,3-dione | HCID 66926174 | 27% |
Reaction Steps
To a microwave vial was added 1,3-cyclopentadione (0.5 g, 5.1 mmol), 6-Chloro-2-(4-chloro-phenyl)-5-methyl-1,6-dihydro-pyrimidine (1.04 g, 4.3 mmol), palladium acetate (58 mg, 0.26 mmol), 2-Dicyclohexylphosphino-2′,4′,6′-triisopropylbiphenyl (183 mg, 0.38 mmol), potassium phosphate tribasic (2.49 g, 11.7 mmol) and 1,4-dioxane (10 ml). This was heated in the microwave for 30 minutes at 150° C. on a normal setting with a pre-stir of 25 seconds. The resulting slurry was diluted with ethyl acetate (10 ml) and 2M hydrochloric acid (10 ml) before filtering through celite. The filter cake was washed with further ethyl acetate (10 ml) and 2M hydrochloric acid (10 ml). The resulting biphasic mixture was separated and the aqueous layer was extracted with further ethyl acetate (2×10 ml). The combined organic layers were then dried with magnesium sulphate, filtered and stripped to dryness to yield a dark yellow solid. This was purified by normal phase chromatography (gradient system of 100% dichloromethane−5% methanol:dichloromethane) to give 2-[2-(4-Chloro-phenyl)-5-methyl-pyrimidin-4-yl]-cyclopentane-1,3-dione as a yellow solid (348 mg, 1.16 mmol, 22% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051300B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-96e9133076d141f8ba4d650d27ce71aa |
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| Source note | uspto-grants-2015_06 |
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