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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110859Generated: November 2, 2026

Potassium Iodide → Methyl 3-isopropoxy-4-methylbenzoate

https://huagongshe.com/reaction/2110859

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) with stirring at room temperature, and the mixture was stirred at 80° C. for 7 hr. 2-Bromopropane (1.79 mL, 19.1 mmol) and potassium iodide (0.27 g, 1.59 mmol) were added to the reaction mixture, and the mixture was further stirred at 80° C. for 15 hr. The reaction mixture was cooled, and diluted with ethyl acetate. The mixture 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. MS (ESI+): 209 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07517910B2
Source datasetuspto-grants-2009_04
ORD IDord-94f4bfe2b786476b80ce4dcf217da9c9
Source noteuspto-grants-2009_04