HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571453Generated: October 26, 2026
Sodium Bicarbonate → 4'-(Fluoro)flavanone
https://huagongshe.com/reaction/571453
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 10719166 | HCID 10719166 | — |
| Reactant | Sodium trifluoromethanesulfonate | HCID 23676748 | — |
| Reactant | HCID 67424417 | HCID 67424417 | — |
| Catalyst | Silver(II) oxide | HCID 92152 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 4'-(Fluoro)flavanone | HCID 11032058 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09024093B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-37709adf6fae437e9ceee66e2eda6c77 |
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| Source note | uspto-grants-2015_05 |
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