HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331388Generated: October 31, 2026
Potassium Carbonate → 5-Methoxy-3-phenyl-1H-inden-1-one
https://huagongshe.com/reaction/331388
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 70310518 | HCID 70310518 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 5-Methoxy-3-phenyl-1H-inden-1-one | HCID 70315592 | 63% |
Reaction Steps
To a solution of (E)-1-(2-bromo-4-methoxyphenyl)-3-phenyl-2-propen-1-one (6.0 g, 18.91 mmol) obtained in Step 2 in DMF (15 mL) was added PPh3 (1.46 g, 5.68 mmol, 0.3 eq), K2CO3 (5.23 g, 37.83 mmol, 2 eq), and PdCl2 (335 mg, 1.89 mmol, 0.1 eq). The reaction vial was heated to 110° C. for 3 h. After cooling to room temperature, the reaction mixture was diluted with EtOAc and filtered through a Celite pad. The solution was washed with H2O and brine, dried over MgSO4, and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexanes=1:5) to afford the desired product (2.8 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877747B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-a0299e06c2004f64b8275a606b3276f7 |
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| Source note | uspto-grants-2014_11 |
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