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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 473002Generated: October 30, 2026

Formaldehyde → 4-fluoro-2-methylene-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/473002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTrifluoroacetic acidHCID 6422—
ReactantPhenylboronic AcidHCID 66827—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Fluoro-1-indanoneHCID 12174986—
SolventTolueneHCID 1140—
Product4-fluoro-2-methylene-2,3-dihydro-1H-inden-1-oneHCID 5819811772%

Reaction Steps

To a 1000 mL round bottle flask were charged 4-fluoro-2,3-dihydro-1H-inden-1-one (249a) (5.04 g, 33.6 mmol), paraformaldehyde (10.08 g, 336 mmol), phenylboronic acid (4.92 g, 40.3 mmol) followed by toluene (235 mL), to the suspension was added TFA 2.6 mL, 33.6 mmol), and the resulting suspension was refluxed for 4 hrs, which resulted a clear yellowish solution. The solution was cooled to room temperature, and the pH was adjusted to 7-8 by adding saturated NaHCO3. After extracting with ethyl acetate, the organic layers were combined, and evaporated. The residue was purified by flash chromatography (0 to 30% EtOAc/Hexane) to give 4-fluoro-2-methylene-2,3-dihydro-1H-inden-1-one (249b) (3.91 g, 72%). LC-MS tR=1.49 min in 3 min chromatography, MS (ESI) m/z 163 [M+H]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08633212B2
Source datasetuspto-grants-2014_01
ORD IDord-81204a30f56c4039b4c1fd6abc0a74e0
Source noteuspto-grants-2014_01