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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Reactant6-bromo-3-methyl-3,4-dihydro-1H-2-benzopyran-1-oneHCID 67516197—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 67517715—

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-f8fc1a36c2e74fa692cd9f0d2c6ac31a
Source noteuspto-grants-2015_06