HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502829Generated: October 28, 2026
Toluene → 5-vinyl-2,3-dihydro-1H-inden-1-one
https://huagongshe.com/reaction/1502829
Participants
| Role | Name | HCID | Charge |
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| Reactant | Toluene | HCID 1140 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-Bromo-1-indanone | HCID 520695 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Product | 5-vinyl-2,3-dihydro-1H-inden-1-one | HCID 67171914 | 48% |
Reaction Steps
To a stirred solution of 5-bromo-2,3-dihydro-1H-inden-1-one (5 g, 23.7 mmol) in toluene were added vinylboronic anhydride pyridine complex (8.55 g, 35.54 mmol), Pd(PPh3)4 (0.1 g, 0.094 mmol), K2CO3 (22.88 g, 165.83 mmol). The resultant reaction mixture was heated at reflux for 16 h. The reaction mixture was cooled to 25° C. and filtered, and the filtrate was concentrated under reduced pressure. The residue was diluted with EtOAc and washed with water and brine. The combined organic extracts were dried over anhydrous Na2SO4 and concentrated under reduced pressure. The obtained residue was purified by flash column chromatography (SiO2, 5% EtOAc in petroleum ether) afforded the title compound as a solid (1.8 g, 48%): 1H NMR (400 MHz, CDCl3) δ 7.74 (d, J=7.2 Hz, 1H), 7.49 (br s, 1H), 7.44 (d, J=7.2 Hz, 1H), 6.82 (m, 1H), 5.90 (d, J=7.4 Hz, 1H), 5.42 (d, J=6.4 Hz, 1H), 3.20 (m, 2H), 2.70 (m, 2H); ESIMS m/z 159.06 ([M+H]−).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09211280B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-5deb12abfa6c43a2afa5ba46a3fe83ed |
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| Source note | uspto-grants-2015_12 |
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