HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718363Generated: October 30, 2026
Potassium Acetate → HCID 123213778, compound
https://huagongshe.com/reaction/718363
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | HCID 118307774 | HCID 118307774 | — |
| Catalyst | Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+) | HCID 178418228 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 123213778 | HCID 123213778 | 39.7% |
Reaction Steps
A mixture of 5-bromo-2-(4-fluorophenethoxy)pyrimidine (200 mg), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (256 mg), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (24.63 mg) and KOAc (198 mg) in 1,4-dioxane (8 mL) in a sealed tube was degassed with nitrogen for 2 minutes and then heated at 85° C. for 4 hours, followed by being stirred at room temperature for 24 h. The mixture was diluted with EtOAc, washed with water, brine, dried over MgSO4 and concentrated under vacuum. The residue was purified by silica gel column (Hex/EtOAc=10:1) to give (2-(4-fluorophenethoxy)pyrimidin-5-yl)boronic acid (70 mg). LCMS (M+H)=263.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193720B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-8b074449efd84b4f9fae53e65d08ab9d |
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| Source note | uspto-grants-2015_11 |
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