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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 850688Generated: October 31, 2026

Methyl iodide → 2-Methoxypropiophenone

https://huagongshe.com/reaction/850688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-1-phenyl-1-propanoneHCID 101121—
SolventAcetoneHCID 180—
SolventDiethyl EtherHCID 3283—
Product2-MethoxypropiophenoneHCID 11309701—

Reaction Steps

A mixture of 2-hydroxypropiophenone (3.00 g, 20.0 mmol), iodomethane (3.40 g, 24.0 mmol), and K2CO3 (granular, anh.; 13.8 g, 99.9 mmol) was refluxed in acetone (75 mL) for 18 h. The reaction mixture was cooled to room temperature and the inorganic salts were removed by filtration. The filtrate was evaporated under vacuum to give an oil which was subsequently dissolved in diethyl ether (200 mL) and then washed with 0.1N NaOH (3×50 mL) followed by H2O (50 ml) The organic layer was dried (anh. Na2SO4), filtered, and evaporated to an orange oil (3.17 g, 96.9%). This material was used in the following step without further purification. TLC, Rf 0.55 (1% MeOH:1% IPA:CHCl3); GC, tr 4.58 min; MS, m/z 164 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06017965
Source datasetuspto-grants-2000_01
ORD IDord-e3dadd7477a64b48ba473891b0f5837e
Source noteuspto-grants-2000_01