HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485545Generated: October 29, 2026
Borane;tetrahydrofuran → 2,4,5,6-Tetrafluoro[1,1'-biphenyl]-3-methanol
https://huagongshe.com/reaction/485545
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Borane;tetrahydrofuran | HCID 2723981 | — |
| Reactant | 2,4,5,6-Tetrafluoro-[1,1'-biphenyl]-3-carboxylic acid | HCID 12853050 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2,4,5,6-Tetrafluoro[1,1'-biphenyl]-3-methanol | HCID 20259239 | — |
Reaction Steps
Under a dry argon atmosphere 2,4,5,6-tetrafluoro-[1,1'-biphenyl]-3-carboxylic acid (21.6 g, 0.08 mole) was dissolved in 150 ml of tetrahydrofuran with stirring. During a 45 minute period 6.9 g of a borane-tetrahydrofuran complex (1.00 molar solution in tetrahydrofuran) was added to the reaction mixture. After complete addition, the reaction mixture was stirred at room temperature for approximately 23 hours. Water (5 ml) was added slowly to the reaction mixture, and the resultant mixture was stirred for two hours. The mixture was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to give a residue, which was dissolved in diethyl ether and water. The organic phase was separated, washed with three 200 ml portions of 2N aqueous sodium hydroxide, and dried over anhydrous magnesium sulfate. Filtration of the mixture and evaporation of the solvent from the filtrate gave 2,4,5,6-tetrafluoro-[1,1'-biphenyl]-3-methanol as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04536591 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-d0c6a3dcd19242568bd4a455580fcbf5 |
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| Source note | uspto-grants-1985_08 |
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