HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173144Generated: October 31, 2026
Triethylamine → 6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-one
https://huagongshe.com/reaction/2173144
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium vinyltrifluoroborate | HCID 23679353 | — |
| Reactant | 6-bromo-3-methyl-3,4-dihydro-1H-2-benzopyran-1-one | HCID 67516197 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-one | HCID 67517715 | — |
Reaction Steps
A solution of 6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-one (2.4 g, 9.96 mmol) and triethylamine (2.78 ml, 19.91 mmol) in EtOH (39.8 ml) was added to a microwave vial containing Cl2Pd(dppf)2-DCM (0.406 g, 0.498 mmol) and potassium vinyltrifluoroborate (2.000 g, 14.93 mmol). The contents of the vial were heated to 100° C. for 1 hour after which the mixture was cooled, diluted with chloroform (50 mL) and washed with aqueous ammonium chloride (25 mL). The organic layer was then dried over magnesium sulfate, filtered and the solvent was evaporated under reduced pressure. MPLC purification (15-60% EtOAc/Hex) gave 6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09056859B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-f8fc1a36c2e74fa692cd9f0d2c6ac31a |
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| Source note | uspto-grants-2015_06 |
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