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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372889Generated: October 30, 2026

Carbon Dioxide → HCID 15180802, compound

https://huagongshe.com/reaction/2372889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
Reactant9-Phenyl-9-(trifluoromethyl)-9H-xanthene-2,7-dicarboxylic acidHCID 15180819—
CatalystCopperHCID 23978—
SolventQuinolineHCID 7047—
ProductHCID 15180802HCID 1518080266%

Reaction Steps

A 6 g sample of 9-phenyl-9-trifluoromethylxanthene-2,7-dicarboxylic acid (XX) was stirred and refluxed i 100 ml quinoline along with 11 g of copper powder, the emanating gas being measured by a wet-test meter. The theoretical amount of CO2 was evolved in two hours. The reaction mixture was cooled, filtered through a bed of Celite into 800 ml of water, acidified wtih 100 ml of concentrated hydrochloric acid, and left standing overnight. The supernatant liquid was decanted, and the residue was taken up in methylene chloride, and filtered through a bed of alumina. The solvent was stripped, the residue was stirred wtih methanol, and was filtered, yielding 3.1 g (66%) of a white solid. It was recrystallized from methanol; m.p. 80°-90°. The IR spectrum was sharp with no OH or CO bands. The NMR spectrum was confirmatory, with the following peaks: d 7.42; m 7.3-7.4; d 7.19, td 6.96, d 6.87 in 2:5:2:2:2 ratio. The compound was analyzed by mass spectrometry which showed the parent ion at 326, along with other peaks, the strongest being at 257 (parent minus trifluoromethyl), and also at 249 (parent minus phenyl), and 199 (parent minus phenyl and minus difluorocarbene). The mass spectrum confirmed the molecular formula as C20H13F3O.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05101004
Source datasetuspto-grants-1992_03
ORD IDord-b29a85feddd34acc8cb37539b4021d74
Source noteuspto-grants-1992_03