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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 322558Generated: October 25, 2026

Methyl iodide → 2-Methoxypropiophenone

https://huagongshe.com/reaction/322558

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 numberUS06211245B1
Source datasetuspto-grants-2001_04
ORD IDord-e15b3a7003e045edadd4160fbd2aa37f
Source noteuspto-grants-2001_04