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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2268548Generated: October 31, 2026

Tetrahydrofuran → 7-[2-(1H-Benzo[d]imidazol-1-yl)ethyl]-2,3-dimethoxy-4,5,6,7,8,9-hexahydro-1H-benzo[a]cycloheptene-1,4-dione

https://huagongshe.com/reaction/2268548

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant2,6-Pyridinedicarboxylic acidHCID 10367—
ReactantCeric ammonium nitrateHCID 180504—
Reactant1-[2-(1,2,3,4-Tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethyl]-1H-benzo[d]imidazoleHCID 18348559—
SolventWaterHCID 962—
SolventSodium BicarbonateHCID 516892—
Product7-[2-(1H-Benzo[d]imidazol-1-yl)ethyl]-2,3-dimethoxy-4,5,6,7,8,9-hexahydro-1H-benzo[a]cycloheptene-1,4-dioneHCID 1834863868.1%

Reaction Steps

To a mixture of 1-[2-(1,2,3,4-tetramethoxy-6,7,8,9-tetrahydro-5H-benzo[a]cyclohepten-7-yl)ethyl]-1H-benzo[d]imidazole (380 mg), pyridine-2,6-dicarboxylic acid (465 mg), THF (8 ml), and water (4 ml) was added an water (4 ml) solution of CAN (2.03 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 saturated aqueous sodium bicarbonate, water, and saturated aqueous sodium chloride and dried. The solvent was removed in vacuo. The residue was recrystallized from ethyl acetate to obtain the entitled compound (240 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06326369B1
Source datasetuspto-grants-2001_12
ORD IDord-a676c70f6e6f4b03b556412fc84be02a
Source noteuspto-grants-2001_12