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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Fluoro-1-indanone | HCID 12174986 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-fluoro-2-methylene-2,3-dihydro-1H-inden-1-one | HCID 58198117 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08633212B2 |
|---|
| Source dataset | uspto-grants-2014_01 |
|---|
| ORD ID | ord-81204a30f56c4039b4c1fd6abc0a74e0 |
|---|
| Source note | uspto-grants-2014_01 |
|---|