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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507981Generated: November 4, 2026

Potassium Iodide → Methyl 3-isopropoxy-4-methylbenzoate

https://huagongshe.com/reaction/507981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant2-BromopropaneHCID 6358—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-hydroxy-4-methylbenzoateHCID 354091—
CatalystPotassium IodideHCID 4875—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-isopropoxy-4-methylbenzoateHCID 2315741296%

Reaction Steps

To a mixture of methyl 3-hydroxy-4-methylbenzoate (5.28 g, 31.8 mmol), potassium carbonate (6.59 g, 47.7 mmol) and N,N-dimethylformamide (50 mL) were added 2-bromopropane (3.58 mL, 38.2 mmol) and potassium iodide (0.53 g, 3.18 mmol) under stirring at room temperature, and the mixture was stirred at 80° C. for 7 hr. To the reaction mixture were added 2-bromopropane (1.79 mL, 19.1 mmol) and potassium iodide (0.27 g, 1.59 mmol), and the mixture was further stirred at 80° C. for 15 hr. The reaction mixture was allowed to cool, diluted with ethyl acetate, washed with water and saturated brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=19/1-hexane/ethyl acetate=4/1) to give the title compound (6.3 g, yield 96%) as a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786165B2
Source datasetuspto-grants-2010_08
ORD IDord-bb2981a1466248789bf2abd202a571d1
Source noteuspto-grants-2010_08