Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401795Generated: October 29, 2026

Boron trifluoride → rel-(3R,4S)-4-(4-Fluorophenyl)tetrahydro-3-furanol

https://huagongshe.com/reaction/401795

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron trifluorideHCID 6356—
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantSodium HydroxideHCID 14798—
Reactant3,6-Dioxabicyclo[3.1.0]hexaneHCID 67511—
ReactantHCID 178418244HCID 178418244—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Productrel-(3R,4S)-4-(4-Fluorophenyl)tetrahydro-3-furanolHCID 5773226439.7%

Reaction Conditions

Temperature-90 °C

Reaction Steps

1.6M BuLi/hexane (399 mL, 0.64 mol, 1.10 eq) was added to a solution of 1-bromo-4-fluorobenzene (70 mL, 0.64 mol, 1.10 eq) in absolute THF (400 mL) in a stream of argon at −90° C. for 1 h. The mixture was stirred at −90° C. for 30 min, cooled to −100° C., and 3,6-dioxabicyclo[3.1.0]hexane (50 g, 0.58 mol, 1 eq) was added. The mixture was stirred at −100° C. for 15 min, and borontrifluoride diethyletherate (81 mL, 0.64 mol, 1.10 eq) was added at the same temperature for 1 h so that the temperature was no higher than −80° C. The reaction mixture was heated to 0° C. for 3 h and diluted with hexane (300 mL) and water (300 mL). 10N sodium hydroxide (50 mL) was added, and the layers were separated. The aqueous layer was extracted with ether. The organic layer was washed with the saturated sodium chloride solution, dried over sodium sulfate, and evaporated. The mixture was subjected to chromatography on silica (1 L, carbon tetrachloride→25, 50, 75, 100% chloroform) to give title compound as a yellow oil (42 g, 0.23 mol, 39.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-f93add8b15df41c0b07e5041e68aa84d
Source noteuspto-grants-2014_06