Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Reactant | 4-Bromo-3-phenyl-1H-pyrazole | HCID 178419463 | — |
| Product | Palladium | HCID 23938 | — |
| Product | 2'-(5-Ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1'-biphenyl]-3-ol | HCID 27282214 | — |
Reaction Steps
The reaction of Example 1 (reaction scale: 10 mmol of bromophenyl pyrazole) was conducted with 0.15 mole % of Pd2(dba)3. After the reaction was judged to be essentially complete, the reaction mixture was neutralized with 1N aq. HCl to a pH of 7.0 to 7.5. After filtration, the crude solid was dissolved in acetone (25 mL/g of bromophenyl pyrazole starting material) at 55° C. TMT (0.05 equiv.) was added, and the mixture was stirred for 1 h while the temperature was allowed to decrease to 30° C. The resulting solution was filtered twice through a Darco zeta pad. The filtrate was concentrated by partial removal of the organic solvents. Recrystallization from acetone/water afforded 2′-(5-ethyl-3,4-diphenyl-1H-pyrazol-1-yl)-[1,1′]-biphenyl-3-ol containing 33 ppm of palladium.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07300639B2 |
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| Source dataset | uspto-grants-2007_11 |
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| ORD ID | ord-5a215d66ecc84afa85219933aae8c0de |
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| Source note | uspto-grants-2007_11 |
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