HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 456227Generated: October 30, 2026
Potassium Carbonate → HCID 44206167, compound
https://huagongshe.com/reaction/456227
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | HCID 86650343 | HCID 86650343 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 44206167 | HCID 44206167 | — |
Reaction Steps
[2′-((4S,5R)-4-Methyl-2-oxo-5-phenyl-oxazolidin-3-ylmethyl)-6-trifluoromethanesulfonyloxy-4′-trifluoromethyl-biphenyl-3-yl]-acetic acid methyl ester (0.100 g, 0.16 mmol), phenylboronic acid (0.029 g, 0.24 mmol), potassium carbonate (0.055 g, 0.40 mmol), and tetrakis(triphenylphosphine)palladium (0) (0.018 g, 0.02 mmol) were combined in DME (2 mL) and H2O (1 mL), and the mixture was purged with N2 for 10 minutes. The reaction was stirred at 90° C. for 5 hours, until no starting material was seen by analytical LCMS. The pH was adjusted to pH 7 with saturated aqueous NH4Cl, and the mixture was extracted with EtOAc. The crude material was purified by silica gel chromatography to give the title compound. M+H is 546.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497381B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-1c026f5b3971441784a051a117907f1f |
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| Source note | uspto-grants-2013_07 |
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