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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248356Generated: October 30, 2026

Methyl iodide → 1-Ethenyl-4-(2-methoxypropan-2-yl)benzene

https://huagongshe.com/reaction/248356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
ReactantBenzenemethanol, 4-ethenyl-α,α-dimethyl-HCID 12542438—
ReactantHCID 178418361HCID 178418361—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-Ethenyl-4-(2-methoxypropan-2-yl)benzeneHCID 1840041651%

Reaction Steps

A solution of 4.10 g of 1-(1-hydroxy-1-methylethyl)-4-ethenyl-benzene in 25 ml of dry tetrahydrofuran containing 7 g of iodomethane was heated to 40°-50° C. and treated portionwise in a dry atmosphere with 1 g of a sodium hydride dispersion (60% NaH in mineral oil) under rapid stirring. Reaction was accompanied by evolution of hydrogen. Once the addition was complete stirring was continued for another 30 minutes. The cooled mixture was then poured into water and extracted with ether. The organic phase was then washed with brine, dried over magnesium sulfate and evaporated to yield a crude product which was purified by preparative HPLO using ethyl acetate-hexane as the eluent to afford 2.25 g (51%) of the desired methyl ether.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05210148
Source datasetuspto-grants-1993_05
ORD IDord-bb1a4b3e50bd490ea74bd707dc78c38b
Source noteuspto-grants-1993_05