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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541336Generated: October 25, 2026

Iodine → Methyl 2-ethyl-5-iodo-4-methylbenzoate

https://huagongshe.com/reaction/541336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantMethyl 2-ethyl-4-methylbenzoateHCID 68288774—
SolventAcetic AcidHCID 176—
ProductMethyl 2-ethyl-5-iodo-4-methylbenzoateHCID 68288177—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a round-bottom flask was added a solution of methyl 2-ethyl-4-methylbenzoate (compound 48.1, 12.5 g, 70.1 mmol, 1.00 equiv) in AcOH (100 mL). NaIO4 (7.51 g, 35.1 mmol, 0.50 equiv) and I2 (21.4 g, 84.3 mmol, 1.20 equiv) were added in portions at 25° C. Sulfuric acid (1.60 g, 16.3 mmol, 0.20 equiv) was then added to the reaction mixture dropwise at 25° C. The resulting solution was stirred for 12 h at 110° C. in an oil bath, and then cooled to ambient temperature. The reaction was quenched with 150 mL of Na2S2O3 (aq., sat.). The aqueous phase was extracted with 2×200 mL of ethyl acetate. The combined organic layers were washed with 3×300 mL of sodium bicarbonate (aq.) and 1×150 mL of brine. The mixture was dried over anhydrous sodium sulfate and concentrated in vacuo. This resulted in 20.0 g (94%) of methyl 2-ethyl-5-iodo-4-methylbenzoate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-3aaccffadd9844638b62eb15574f7f72
Source noteuspto-grants-2014_10