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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1501308Generated: November 3, 2026

Benzophenone → HCID 102108769, compound

https://huagongshe.com/reaction/1501308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzophenoneHCID 3102—
ReactantQuinolineHCID 7047—
Reactant18-Crown-6HCID 28557—
ReactantPotassium FluorideHCID 522689—
Reactant2-(Trimethylsilyl)phenyl trifluoromethanesulfonateHCID 3384007—
SolventTetrahydrofuranHCID 8028—
ProductHCID 102108769HCID 10210876954.2%

Reaction Steps

Following the general procedure, treatment of quinoline (0.064 g, 59 μL, 0.50 mmol) and benzophenone (0.136 g, 0.75 mmol) with 2-(trimethylsilyl)phenyl trifluoromethanesulfonate (0.179 g, 146 μL, 0.60 mmol) in the presence of KF (0.070 g, 1.2 mmol) and 18-crown-6 (0.317 g, 1.2 mmol) in THF (2.0 mL) at −10° C. to room temperature for 12 hrs followed by flash column chromatography (Pet. ether/EtOAc=95/05) of the crude reaction mixture afforded 5,5-diphenyl-5H,6aH-benzo[4,5][1,3]oxazino[3,2-a]quinoline as a yellow solid (0.105g, 54% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09206196B1
Source datasetuspto-grants-2015_12
ORD IDord-b95fe09b3f9e4c5881bd30db8f23f601
Source noteuspto-grants-2015_12