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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1085928Generated: November 1, 2026

Quinone → HCID 20059337, compound

https://huagongshe.com/reaction/1085928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantQuinoneHCID 4650—
ReactantHCID 14642797HCID 14642797—
CatalystManganese dioxideHCID 14801—
SolventChloroformHCID 6212—
Solvent1,2-DichlorobenzeneHCID 7239—
ProductHCID 20059337HCID 20059337—

Reaction Steps

23.47 g (0.1011 mol) of 4,5-bis-trifluoromethyl-2-oxo-2H-pyran, 54.62 g (0.5053 mol) of 1,4-benzoquinone and 26.30 g (0.3026 mol) of MnO2 in 225 ml of 1,2-dichlorobenzene are heated at 180° C. for 12 hours. The reaction mixture is then diluted with 200 ml of CHCl3 and filtered through Hyflo®. After the chloroform has been removed by distillation, the distillation residue is chromatographed over a column packed with 1300 g of SiO2 (mobile phase: first cyclohexane and then CHCl3 ; 0.3 bar excess pressure). Yield 17.94 g (60.3%), melting point: 91°-94° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05011944
Source datasetuspto-grants-1991_04
ORD IDord-cacb4a8e3e094ec5bdba530aeffe4f0b
Source noteuspto-grants-1991_04