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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1909857Generated: November 2, 2026

Tetrahydrofuran → HCID 66868239, compound

https://huagongshe.com/reaction/1909857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant5-Chloro-2-nitrobenzaldehydeHCID 81123—
ReactantHCID 19988374HCID 19988374—
ReactantPotassium tert-butoxideHCID 23665647—
SolventWaterHCID 962—
ProductHCID 66868239HCID 6686823949.7%

Reaction Steps

To a mixture of (3-oxo-1,3-dihydro-2-benzofuran-1-yl)(triphenyl) phosphonium bromide (5.1 g) and tetrahydrofuran (50 mL) were added potassium tert-butoxide (1.3 g) and 5-chloro-2-nitro benzoaldehyde (1.0 g) at room temperature under an argon atmosphere, followed by stirring for 5 minutes. To the reaction mixture was added water, followed by extraction with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane-ethyl acetate) to obtain 3-(5-chloro-2-nitrobenzylidene)-2-benzofuran-1(3H)-one (808 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598355B2
Source datasetuspto-grants-2013_12
ORD IDord-0a7be9bcdac04d308ed733918b1eda8f
Source noteuspto-grants-2013_12