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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2175779Generated: October 29, 2026

Triethylamine → (3R)-6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-one

https://huagongshe.com/reaction/2175779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium vinyltrifluoroborateHCID 23679353—
Reactant(3R)-6-bromo-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 71270763—
CatalystHCID 178418807HCID 178418807—
SolventEthanolHCID 702—
SolventChloroformHCID 6212—
Product(3R)-6-ethenyl-3-methyl-3,4-dihydro-1H-isochromen-1-oneHCID 86727028—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of (3R)-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 PdCl2(dppf)-CH2Cl2, (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 the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062070B2
Source datasetuspto-grants-2015_06
ORD IDord-2c87f7dd17364c469e60885b8bca03df
Source noteuspto-grants-2015_06