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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron trifluoride | HCID 6356 | — |
| Reactant | 1-Bromo-4-fluorobenzene | HCID 9993 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3,6-Dioxabicyclo[3.1.0]hexane | HCID 67511 | — |
| Reactant | HCID 178418244 | HCID 178418244 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | rel-(3R,4S)-4-(4-Fluorophenyl)tetrahydro-3-furanol | HCID 57732264 | 39.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741934B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-f93add8b15df41c0b07e5041e68aa84d |
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| Source note | uspto-grants-2014_06 |
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