Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1065564Generated: November 1, 2026

Borane;tetrahydrofuran → 2,4,5,6-Tetrafluoro[1,1'-biphenyl]-3-methanol

https://huagongshe.com/reaction/1065564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBorane;tetrahydrofuranHCID 2723981—
Reactant2,4,5,6-Tetrafluoro-[1,1'-biphenyl]-3-carboxylic acidHCID 12853050—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product2,4,5,6-Tetrafluoro[1,1'-biphenyl]-3-methanolHCID 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 (0.001 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 2 N 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04329518
Source datasetuspto-grants-1982_05
ORD IDord-732ebf659d824a79a19ca01979fb05aa
Source noteuspto-grants-1982_05