HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362781Generated: October 30, 2026
Tetrahydrofuran → Methyl (2'-fluoro[1,1'-biphenyl]-4-yl)acetate
https://huagongshe.com/reaction/1362781
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Methyl 2-(4-bromophenyl)acetate | HCID 316783 | — |
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl (2'-fluoro[1,1'-biphenyl]-4-yl)acetate | HCID 12094240 | — |
Reaction Steps
47.6 g (0.21 mol) of methyl 4-bromophenylacetate are introduced under argon into 400 ml of absolute tetrahydrofuran and, at room temperature, 320 ml of 1M sodium carbonate solution and 40 g (0.28 mol) of 2-fluorophenylboronic acid are added. Addition of 7.0 g (0.01 mol) of bis(triphenylphosphane)palladium(II) chloride is followed by heating under reflux for 18 h. Cooling is followed by dilution with 500 ml of water and extracted three times with 300 ml of ethyl acetate each time. The combined organic phases are washed with 400 ml each of saturated ammonium chloride solution, water and saturated sodium chloride solution, dried over magnesium sulfate and freed of solvent in vacuo. Example V is obtained after silica gel filtration (petroleum ether/ethyl acetate 10:1) as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07883713B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-d0226dd4d3544808a278e6edf9d8e5c6 |
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| Source note | uspto-grants-2011_02 |
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