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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268553Generated: November 1, 2026

Tetrahydrofuran → 2,3-Dimethoxy-7-[2-(2-quinolyloxy)ethyl]-4,5,6,7,8,9-hexahydro-1H-benzo[a]cycloheptene-1,4-dione

https://huagongshe.com/reaction/2268553

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,6-Pyridinedicarboxylic acidHCID 10367—
ReactantCeric ammonium nitrateHCID 180504—
Reactant2-[2-(1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethoxy]quinolineHCID 18348511—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product2,3-Dimethoxy-7-[2-(2-quinolyloxy)ethyl]-4,5,6,7,8,9-hexahydro-1H-benzo[a]cycloheptene-1,4-dioneHCID 1834857164.8%

Reaction Steps

To a mixture of 2-[2-(1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethoxy]quinoline (580 mg), pyridine-2,6-dicarboxylic acid (667 mg), THF (18 ml), and water (6 ml) was added an water (6 ml) solution of CAN (2.92 g) with cooling with ice. After being stirred for 15 min, the reaction mixture was diluted with saturated aqueous sodium bicarbonate and extracted with ethyl acetate. The organic layer was washed with water and saturated aqueous sodium chloride and dried. The solvent was removed in vacuo and the residue was recrystallized from ethyl acetate to obtain the entitled compound (350 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326369B1
Source datasetuspto-grants-2001_12
ORD IDord-16b4a0e75377420a8eb36e5745abfec1
Source noteuspto-grants-2001_12