HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918735Generated: November 1, 2026
3-Bromoquinoline → HCID 178519901, compound
https://huagongshe.com/reaction/918735
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Bromoquinoline | HCID 21413 | — |
| Reactant | 1,3-Oxazol-4-ylmethanol | HCID 15930578 | — |
| Reagent | Potassium Trimethylacetate | HCID 23662159 | — |
| Catalyst | Bromo(thiobis(methane))copper | HCID 2724234 | — |
| Catalyst | Dichloro-[1,3-bis(diisopropylphenyl)-2-imidazolidinyliden]-(3-chloropyridyl)palladium(II) | HCID 16218181 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178519901 | HCID 178519901 | — |
| Product | HCID 178519952 | HCID 178519952 | — |
| Product | HCID 178520002 | HCID 178520002 | — |
Reaction Steps
- reaction input `pd_catalyst` was added as a solution (2-methyltetrahydrofuran 1 mmol/L) and then the solvent was removed to leave solid solute before adding other reactants/reagents; - stirrer was added after `pd_catalyst` and before `base`; - reaction inputs were prepared inside a glove box but the reaction itself did not happen in a glove box; - the reaction vial was sealed after adding all reaction inputs
Provenance & Evidence
| DOI | 10.1039/d3dd00167a |
|---|
| Source dataset | C-H activation of oxazoles from the second demo case in the PyParser paper |
|---|
| ORD ID | ord-3f725689f519483fa7f0882e508cbe89 |
|---|
| Source note | C-H activation of oxazoles from the second demo case in the PyParser paper |
|---|
