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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383520Generated: October 31, 2026

Tetrahydrofuran → HCID 58926072, compound

https://huagongshe.com/reaction/383520

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMorpholineHCID 8083—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-6-fluoro-1,3-dihydro-2H-indol-2-oneHCID 58926029—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 58926072HCID 58926072—

Reaction Conditions

Temperature108 °C

Reaction Steps

A pressure tube was charged with (3E)-3-(4-bromo-5,5-dimethylfuran-2(5H)-ylidene)-6-fluoro-1,3-dihydro-2H-indol-2-one (60 mg, 0.19 mmol), morpholine (48 mg, 0.56 mmol), Mo(CO)6 (49 mg, 0.19 mmol), palladium(II) acetate (4.0 mg, 0.018 mmol), DBU (85 mg, 0.56 mmol) and anhydrous THF (3 mL). The tube was immediately capped under nitrogen and heated in 108° C. bath for 1 hour. After cooling, the reaction mixture was filtered through a short celite pad. The filtrate was concentrated and purified by silica gel flash chromatography (5-10% MeOH in CHCl3) to give (3E)-3-[5,5-dimethyl-4-(morpholin-4-ylcarbonyl)furan-2(5H)-ylidene]-6-fluoro-1,3-dihydro-2H-indol-2-one as a yellow solid. Yield: 39 mg, 55%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367664B2
Source datasetuspto-grants-2013_02
ORD IDord-6320f7ef7e9c411db85688fa314dd962
Source noteuspto-grants-2013_02