HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2059878Generated: November 2, 2026
Potassium Phosphate, Tribasic → (E)-4-chloro-6-(4-chlorostyryl)pyrimidine
https://huagongshe.com/reaction/2059878
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 4,6-Dichloropyrimidine | HCID 70943 | — |
| Reactant | trans-2-(4-Chlorophenyl)vinylboronic acid | HCID 642694 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (E)-4-chloro-6-(4-chlorostyryl)pyrimidine | HCID 58579925 | 24.4% |
Reaction Steps
A mixture of commercially available 4,6-dichloropyrimidine (300 mg, 2.01 mmol), (E)-4-chlorostyrylboronic acid (441 mg, 2.41 mmol), potassium phosphate (1282 mg, 6.04 mmol), and PalladiumTetrakis (116 mg, 0.10 mmol) in DMF (1 mL) was stirred under nitrogen at 40° C. for 2 days. The reaction was filtered, diluted with CH2Cl2, washed with water, brine, dried (MgSO4), and concentrated. The crude product was purified using ISCO flash chromatography (silica gel/hexanes/ethyl acetate 100:0 to 50:50 gradient) to afford the desired product (E)-4-chloro-6-(4-chlorostyryl)pyrimidine 20A (120 mg, 0.49 mmol, 23.73% yield) as a light yellow solid. LC/MS 252 (M+H)+, tR 1.07 min (method 5).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278316B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-5c24e7569c4f40c9ba07ab9d1abe1618 |
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| Source note | uspto-grants-2012_10 |
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