HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 15355Generated: October 29, 2026
Water → 7-Vinyl-3,4-dihydroisoquinolin-1(2H)-one
https://huagongshe.com/reaction/15355
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Trivinylboroxin | HCID 2734807 | — |
| Reactant | 7-Bromo-3,4-dihydroisoquinolin-1(2H)-one | HCID 25067330 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | 7-Vinyl-3,4-dihydroisoquinolin-1(2H)-one | HCID 57486895 | 88% |
Reaction Steps
A solution of 7-bromo-3,4-dihydro-1(2H)-isoquinolinone (0.679 g, 3.004 mmol) and tetrakis(triphenylphosphine)palladium(0) (174 mg, 0.150 mmol) in 1,2-dimethoxyethane (30 ml) was stirred at room temperature for 0.5 h before addition of 2,4,6-trivinylcyclotriboroxane.pyridine complex (for a synthesis see Kerins, Fergal; O'Shea, Donal F. J. Org. Chem. (2002), 67(14), 4968) (295 mg, 1.218 mmol), K2CO3 (415 mg, 3.004 mmol) and water (10 ml). The reaction was heated at reflux for 1.5 h before cooling to room temperature and addition of water (50 ml). The mixture was extracted with 10% methanol/dichloromethane (3×100 ml), the organic layers were dried with magnesium sulphate and evaporated. Chromatography on silica, eluting with 0-100% ethyl acetate/hexane, gave the product (456 mg, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07732461B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-1ec7c15c01e6444397a75d5fcb662fec |
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| Source note | uspto-grants-2010_06 |
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