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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1466114Generated: November 3, 2026

Tri-tert-butylphosphine tetrafluoroborate → 6-(1,3-Dioxolan-2-ylmethyl)-3,4-dihydroisochromen-1-one

https://huagongshe.com/reaction/1466114

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
Reactant6-bromo-3,4-dihydro-1H-2-benzopyran-1-oneHCID 44130843—
ReactantHCID 178419777HCID 178419777—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
Product6-(1,3-Dioxolan-2-ylmethyl)-3,4-dihydroisochromen-1-oneHCID 67517374—

Reaction Conditions

Temperature85 °C

Reaction Steps

6-bromo-3,4-dihydro-1H-isochromen-1-one (10 g, 44 mmol) was combined with tri-t-butyl phosphonium tetrafluoroborate (256 mg, 0.881 mmol), palladium (II) acetate (99 mg, 0.44 mmol) and commercially available bromo(1,3-dioxolan-2-ylmethyl)zinc solution (0.5 M, 97 mL, 48 mmol) in DMF (100 mL), and the mixture was degassed three times by alternating vacuum and nitrogen purge. The mixture was then heated at 85° C. for 6 h, then was stirred at RT overnight. Ethyl acetate and ether were added and the mixture was washed with water. The aqueous layer was extracted with ethyl acetate, the organic layers were combined, and washed twice with water and once with brine. The organic layer was dried over MgSO4, filtered and concentrated. The crude product was purified by MPLC (silica) eluting with ethyl acetate in hexanes to afford the title compound. LCMS: m/z 235 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999990B2
Source datasetuspto-grants-2015_04
ORD IDord-5cb41f3a357142578481943aedb1d0e3
Source noteuspto-grants-2015_04