HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 33282Generated: October 29, 2026
Sodium Carbonate → HCID 86587705, compound
https://huagongshe.com/reaction/33282
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | 2-Bromo-3,4-dihydropyrrolo[4,3,2-de]isoquinolin-5-(1H)-one | HCID 9881439 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 86587705 | HCID 86587705 | 93.1% |
Reaction Steps
To a suspension of 2 (0.1065 g, 0.424 mmol) in 20 mL toluene/10 mL EtOH was added phenylboronic acid (0.08 g, 0.636 mmol), Na2CO3 (0.113 g, 1.06 mmol) dissolved in a minimum amount of water, LiCl (0.054 g, 1.27 mmol), and tetrakis(triphenylphosphine)palladium(0) (24.5 mg, 21.0 μmol). The reaction mixture was refluxed for 16 h. The solvent was removed in vacuo, and the residue was taken up in EtOAc and washed with saturated aqueous NaHCO3, H2O, and brine. The organic layer was dried over Na2SO4 and concentrated to give a yellow solid, which was purified by flash column chromatography eluting with a gradient of 20% of EtOAc in hexanes to give 0.098 g of a mixture of 3 as a yellow solid. mp 215-218° C. (dec); 1H NMR (DMSO-d6) δ 5.04 (s, 2H), 7.17 (t, 1H, J=7.5 Hz), 7.34 (d, 1H, J=6.6 Hz), 7.35 (d, 1H, J=7.4 Hz), 7.50 (m, 4H), 7.66 (d, 1H, J=7.7 Hz), 7.84 (s, 1H), 11.64 (s, 1H); HRMS (M+H) 249.1023.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07429578B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-45c2e9abb764453ab52c7cafac6aa0b6 |
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| Source note | uspto-grants-2008_09 |
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