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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571453Generated: October 26, 2026

Sodium Bicarbonate → 4'-(Fluoro)flavanone

https://huagongshe.com/reaction/571453

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 10719166HCID 10719166—
ReactantSodium trifluoromethanesulfonateHCID 23676748—
ReactantHCID 67424417HCID 67424417—
CatalystSilver(II) oxideHCID 92152—
SolventAcetoneHCID 180—
Product4'-(Fluoro)flavanoneHCID 1103205890%

Reaction Conditions

Temperature65 °C

Reaction Steps

To 4′-(Trifluoromethanesulfonyl)flavanone (51.4 mg, 0.100 mmol, 1.00 equiv) in acetone (2.0 mL) at 23° C. was added silver oxide (1.16 mg, 0.00500 mmol, 0.05 equiv), sodium bicarbonate (16.8 mg, 0.200 mmol, 2.00 equiv), sodium trifluoromethanesulfonate (17.2 mg, 0.100 mmol, 1.00 equiv) and 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(hexafluorophosphate) (2) (70.5 mg, 0.150 mmol, 1.50 equiv). The reaction mixture was stirred for 5 h at 65° C. in a sealed vial, then cooled to 23° C. and concentrated in vacuo. The residue was purified by preparative TLC with hexane/EtOAc 5:1 (v/v) to afford 21.8 mg of the title compound as a white solid (90% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024093B2
Source datasetuspto-grants-2015_05
ORD IDord-37709adf6fae437e9ceee66e2eda6c77
Source noteuspto-grants-2015_05