Suzuki–Miyaura coupling, record ord-3f88326c0f374759bee97dd6cc27f550
One recorded run of this reaction. Below is what the source recorded, and nothing added to it.
What was in the flask
| Role | Species | Formula | Yield |
|---|---|---|---|
| Reactant | 4-Chloroanisole | C₇H₇ClO | |
| Reactant | Phenylboronic Acid | C₆H₇BO₂ | |
| Reagent | Water | H₂O | |
| Reagent | Potassium Phosphate, Tribasic | K₃O₄P | |
| Catalyst | Bis(1,5-cyclooctadiene)nickel | C₁₆H₂₄Ni | |
| Catalyst | PnButBu2 | C₁₂H₂₇P | |
| Solvent | 1,4-Dioxane | C₄H₈O₂ | |
| Solvent | 1,4-Dioxane | C₄H₈O₂ | |
| Solvent | 1,4-Dioxane | C₄H₈O₂ | |
| Solvent | 1,4-Dioxane | C₄H₈O₂ | |
| Product | 4-Methoxybiphenyl | C₁₃H₁₂O | 4% |
Conditions
- Temperature
- 60 °C
- Duration
- 2 hours
Yield
- 4% of 4-Methoxybiphenyl.
Procedure
Copied from the source record, unedited
pre-ligate Ni(cod)2 and phosphine ligand in dioxane for 15 minutes in a separate plate
The source
This record comes from experimental reaction archive (ord-3f88326c0f374759bee97dd6cc27f550). Open the source and check it against what is on this page.
experimental reaction archive record ord-3f88326c0f374759bee97dd6cc27f550 from dataset "Ni-catalyzed Suzuki Miyaura cross-coupling" (doi: 10.26434/chemrxiv.14388557.v1). No atom mapping is provided by the source.
How to read this record
This is one experiment, not a rule. It says that on one occasion these species were combined under these conditions and this came out. It does not say the reaction will give the same result on your substrate, and nothing on the page has been generalised into a claim that it would.
The pathway is a separate question, kept on separate pages. A mechanism here is the canonical arrow pushing for a class, run on real structures and labelled rule-derived. It is not evidence, and this record is not a mechanism.