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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2165006Generated: November 2, 2026

Methyl iodide → 2,2-Bis(2-methoxyphenyl)butane

https://huagongshe.com/reaction/2165006

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantTetrahydrofuranHCID 8028—
Reactant1,1-Bis(2-methoxyphenyl)etheneHCID 4639283—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product2,2-Bis(2-methoxyphenyl)butaneHCID 19812693—

Reaction Steps

1,1-Bis(2-methoxyphenyl)ethene (5.6 g) was dissolved in 25 ml of tetrahydrofuran and 25 ml of a 1.3M solution of methyl lithium in ether was added dropwise with stirring. The solution became dark red and exothermed. After 2 hours, 5.0 ml of methyl iodide was added slowly with stirring. The solution again exothermed. When all of the methyl iodide had been added the starting material was found to be completely consumed and replaced by a single product by gas-liquid chromatography. About 300 ml of ether was added and the resulting solution was extracted with 100 ml of water and then 100 ml of brine, dried over magnesium sulfate, filtered, and concentrated by evaporation under reduced pressure to obtain 5.46 g (88 percent of theory) of the title compound as a pale yellow crystalline solid melting at 49-52° C. The proton and carbon NMR and infrared spectra were consistent with the assigned structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04938790
Source datasetuspto-grants-1990_07
ORD IDord-d3d17d23dc7d4a50823c1aed5090dc50
Source noteuspto-grants-1990_07