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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541369Generated: October 30, 2026

Iodine → Methyl 4-cyclopropyl-2-ethyl-5-iodobenzoate

https://huagongshe.com/reaction/541369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantMethyl 4-cyclopropyl-2-ethylbenzoateHCID 68288825—
SolventAcetic AcidHCID 176—
ProductMethyl 4-cyclopropyl-2-ethyl-5-iodobenzoateHCID 6828885749.5%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a round-bottom flask was added a solution of methyl 4-cyclopropyl-2-ethylbenzoate (compound 226.3, 5.00 g, 24.5 mmol, 1.00 equiv) in AcOH (40 mL). I2 (6.80 g, 26.8 mmol, 1.10 equiv), NaIO4 (2.60 g, 12.2 mmol, 0.50 equiv), and sulfuric acid (400 mg, 4.08 mmol, 0.15 equiv) were added to the reaction. The resulting solution was stirred for 2 h at 50° C. After cooling to ambient temperature, the reaction was carefully quenched with Na2S2O3 (aq., sat.). The mixture was extracted with 2×100 mL of ethyl acetate, and the combined organic layers were dried over sodium sulfate and concentrated in vacuo. The residue was purified using silica gel column chromatography with petroleum ether/ethyl acetate (20:1) as eluent to furnish 4.00 g (49%) of methyl 4-cyclopropyl-2-ethyl-5-iodobenzoate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-3f532688706c45dda5eddea1fd31253f
Source noteuspto-grants-2014_10