HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1399559Generated: October 26, 2026
1,2-Dimethoxyethane → Methyl 2-(2-chloro-4-methyl-6-phenylpyrimidin-5-yl)acetate
https://huagongshe.com/reaction/1399559
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Methyl 2-(2,4-dichloro-6-methylpyrimidin-5-yl)acetate | HCID 19044674 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-(2-chloro-4-methyl-6-phenylpyrimidin-5-yl)acetate | HCID 86665645 | 66.1% |
Reaction Steps
To a suspension of methyl 2-(2,4-dichloro-6-methylpyrimidin-5-yl)acetate (4.42 g; 18.80 mmol) in a mixture of degassed DME (75 mL) and water (25 mL) was added phenyl boronic acid (5.73 g; 47 mmol), Tetrakis(triphenylphosphine) palladium(0) (2 g; 1.731 mmol) and diisopropyl ethylamine (12.96 mL; 75 mmol). The reaction was stirred under reflux for 3.5 h. The reaction mixture was partitioned between brine and ethyl acetate. The phases were separated and the water layer was extracted with ethyl acetate. The combined organic layers were dried over magnesium sulphate and concentrated under reduced pressure. The crude material was purified by flash chromatography on silica gel using a linear gradient of ethylacetate (5-40%) in heptane to give 3.44 g (65%) of the title compound as a white solid. ESI/APCI(+): 277 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906906B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-a6d5a5b1e1ea46c59d108181722b0863 |
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| Source note | uspto-grants-2014_12 |
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