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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766646Generated: October 30, 2026

Methane, dichloromethoxy- → 2-Methoxy-5-(5-methyl-7-nitroindan-4-yloxy)benzaldehyde

https://huagongshe.com/reaction/1766646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethane, dichloromethoxy-HCID 21004—
Reactant2,3-Dihydro-4-(4-methoxyphenoxy)-5-methyl-7-nitro-1H-indeneHCID 23031114—
CatalystTitanium TetrachlorideHCID 24193—
SolventDichloromethaneHCID 6344—
Product2-Methoxy-5-(5-methyl-7-nitroindan-4-yloxy)benzaldehydeHCID 23031205—

Reaction Steps

4-(4-methoxyphenoxy)-5-methyl-7-nitroindane (5.0 g) and dichloromethyl methyl ether (3.02 mL) were dissolved in dichloromethane (50 mL). To the solution was added dropwise titanium tetrachloride (3.67 mL) under ice-cooling with stirring. The reaction mixture was stirred at room temperature under an argon atmosphere for 20 hours. After adding ice water (300 mL), the reaction mixture was extracted with ethyl acetate. The organic layer was washed with a saturated aqueous solution of sodium hydrogen carbonate and brine successively, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure. The residue was triturated with hexane (50 mL) and diethyl ether (5 mL), and the insoluble material was collected by filtration and washed with hexane to give the title compound (4.37 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230031B2
Source datasetuspto-grants-2007_06
ORD IDord-e1ac0c6ed2244fd2afa6481a2c629b3e
Source noteuspto-grants-2007_06