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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527670Generated: October 26, 2026

Methyl iodide → 1,2,3,4-Tetramethoxybenzene

https://huagongshe.com/reaction/1527670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant2,3,4-TrimethoxyphenolHCID 603577—
SolventAcetoneHCID 180—
Product1,2,3,4-TetramethoxybenzeneHCID 60777382.3%

Reaction Steps

Following the procedure by Tremblay et al.,17 17 (3.851 g, 20.9 mmol) was dissolved in dry acetone (90.0 ml), and K2CO3 (9.36 g, 67.7 mmol) was added followed by MeI (9.0 mL, 144 mmol). The reaction was heated under reflux for 26 h and monitored by TLC (1:9 EtOAc:hexanes) for completion. When complete the reaction was cooled to room temperature and filtered. The acetone was removed under reduced pressure and the residue was taken up in CH2Cl2 (50 mL). The suspension was filtered, dried over MgSO4, filtered again, and condensed. The crude product can be purified by flash chromatography (1:4 EtOAc:hexanes), however, recrystallization from Et2O/hexanes was sufficient to provide pure 18 (3.405 g, 17.2 mmol, 82%) as white needles.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09089605B2
Source datasetuspto-grants-2015_07
ORD IDord-160a9da54c0247b199edd594e23558a2
Source noteuspto-grants-2015_07