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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1039277Generated: November 4, 2026

Methyl iodide → 4-Bromo-7-methoxy-6-nitro-2,3-dihydro-1H-inden-1-one

https://huagongshe.com/reaction/1039277

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantSodium BicarbonateHCID 516892—
Reactant4-Bromo-7-hydroxy-6-nitro-2,3-dihydro-1H-inden-1-oneHCID 57781233—
SolventDimethylformamideHCID 6228—
Product4-Bromo-7-methoxy-6-nitro-2,3-dihydro-1H-inden-1-oneHCID 5778126379%

Reaction Steps

4-Bromo-7-hydroxy-6-nitroindan-1-one (8.07 g, 29.7 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (5.33 mL, 35.6 mmol) were dissolved in N,N-dimethylformamide (150 mL), iodomethane (18.5 mL, 297 mmol) was added, and the mixture was stirred at room temperature for 40 hr. To the reaction solution was added saturated aqueous sodium hydrogencarbonate solution. The mixture was extracted with diethyl ether, washed with saturated brine and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=30/70→60/40) to give the title compound (6.70 g, yield 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08552037B2
Source datasetuspto-grants-2013_10
ORD IDord-806e464ca38a4027b362e9c9ad85351c
Source noteuspto-grants-2013_10