HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283699Generated: November 1, 2026
Potassium Phosphate, Tribasic → HCID 818966, compound
https://huagongshe.com/reaction/2283699
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-Chloropyrimidine | HCID 74404 | — |
| Reactant | Thiophene-3-boronic acid | HCID 581760 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 2-Methyl-2-butanol | HCID 6405 | — |
| Product | HCID 818966 | HCID 818966 | — |
Reaction Steps
Tert-amyl alcohol (100 mL) was added to tris(dibenzylideneacetone)dipalladium(0) (460 mg), 2-(dicyclohexylphosphino)-2′,4′,6′-triisopropyl-1,1′-biphenyl (960 mg), 3-thiophene boronic acid (9.60 g), 2-chloropyrimidine (5.72 g), potassium phosphate (21.2 g), and molecular sieve 4 A (12.5 g). The reaction solution was stirred at 100° C. overnight. The insolubles were filtrated, and then the solvent was evaporated under vacuum. The resultant residue was purified by column chromatography on silica gel (developing solvent:hexane/ethyl acetate) to obtain 2-(thiophen-3-yl) pyrimidine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145414B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-c22153ff99eb448ab4123cf48fb0d797 |
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| Source note | uspto-grants-2015_09 |
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