HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2261111Generated: October 30, 2026
Water → 5-(1,3-Dioxolan-2-yl)-2-fluoro-1-benzofuran
https://huagongshe.com/reaction/2261111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | N-Fluorobenzenesulfonimide | HCID 588007 | — |
| Reactant | 5-(1,3-Dioxolan-2-yl)-1-benzofuran | HCID 55255325 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-(1,3-Dioxolan-2-yl)-2-fluoro-1-benzofuran | HCID 57469679 | 138.6% |
Reaction Steps
5-[1,3]Dioxolan-2-yl-benzofuran (50 mg, 0.26 mmol) was dissolved in THF (2 mL) and the solution was cooled down to −78° C. Butyl lithium (180 uL, 1.1 eq.) was added dropwise. This mixture was stirred 30 min at 25° C. Then the reaction mixture was cooled down to −78° C. and N-fluorodibenzenesulfonamide (91 mg, 1.1 eq.), dissolved in 1 mL THF, was added dropwise to the reaction mixture. The mixture was stirred overnight between −78° C. and room temperature. Water and ethyl acetate were added to the mixture and the aqueous layer was extracted 3 times. Combined organic phases was dried over MgSO4, filtrated and evaporated, to give the 2-Fluoro-5-[1,3]dioxolan-2-yl-benzofuran (75 mg) mixed with side products. However it was sufficiently pure to be used for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07846925B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-6a9e062841174572a640a721fa576c5e |
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| Source note | uspto-grants-2010_12 |
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