HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2234147Generated: October 30, 2026
1,1'-Biphenyl-4-yl-boronic acid → HCID 66760170, compound
https://huagongshe.com/reaction/2234147
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,1'-Biphenyl-4-yl-boronic acid | HCID 151253 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | {4-[3,3-Bis-(4-bromo-phenyl)-allylsulfanyl]-2-methyl-phenoxy}-acetic acid | HCID 10370262 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Product | HCID 66760170 | HCID 66760170 | — |
Reaction Steps
A mixture of {4-[3,3-bis-(4-bromo-phenyl)-allylsulfanyl]-2-methyl-phenoxy}-acetic acid (example 1) (225 mg, 0.410 mmol), 4-biphenylboronic acid (163 mg, 0.82 mmol), KF (79 mg, 1.35 mmol), Pd2(dba)3 (23 mg, 0.025 mmol) and Pd(P(t-Bu)3)2 (25 mg, 0.049 mmol) was evacuated for air and kept under nitrogen. THF (6 ml) was added and the reaction mixture was stirred at 70° C. overnight. A saturated aqueous NH4Cl (5 ml) solution was added, and the mixture was extracted with methylene chloride (2×20 ml). The combined organic phases were dried an evaporated. The isolated products were further purified on column chromatography using methylene chloride:THF (40:1) as eluent. The isolated products were further purified on HPLC using acetonitril:water (7:3) increasing to pure acetonotril as eluent. The title product was isolated as an E/Z mixture in 40 mg (16%) yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07709528B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-635bc1c25b104fe6ad70c45a92ae8053 |
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| Source note | uspto-grants-2010_05 |
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