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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941153Generated: October 26, 2026

Sodium hydride → 2-[2-(3,4-Dimethoxyphenyl)ethoxy]-7-hydroxymethyl-4-isopropyl-2,4,6-cycloheptatrien-1-one

https://huagongshe.com/reaction/1941153

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant4-(2-Iodoethyl)-1,2-dimethoxybenzeneHCID 597022—
ReactantHCID 178439170HCID 178439170—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product2-[2-(3,4-Dimethoxyphenyl)ethoxy]-7-hydroxymethyl-4-isopropyl-2,4,6-cycloheptatrien-1-oneHCID 2145993811%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 2-hydroxy-7-hydroxymethyl-4-isopropyl-2,4,6-cycloheptatrien-1-one (844 mg, 4.35 mmol) in dimethylformamide (5 ml) was stirred while 60% oily sodium hydride (191 mg, 4.78 mg) in small portions were added thereto. Subsequently, 3,4-dimethoxyphenethyl iodide (2.54 mg, 8.70 mmol) was added, then the solution was heated at 80° C. for 7 hours. The solution was diluted with dichloromethane, washed with water and dried over sodium sulfate. After solvent was distilled off under reduced pressure, the residue was purified by silica gel column chromatography [eluent: hexane/ethyl acetate (3:2)] to give 169 mg of 2-[2-(3,4-dimethoxyphenyl)ethoxy]-7-hydroxymethyl-4-isopropyl-2,4,6-cycloheptatrien-1-one as a yellowish brown oil (yield: 11%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05703071
Source datasetuspto-grants-1997_12
ORD IDord-d2ff51f69fd84d13940369a3602bc635
Source noteuspto-grants-1997_12