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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 541306Generated: October 30, 2026

Iodine → Methyl 4-(cyclobutylmethyl)-5-iodo-2-methylbenzoate

https://huagongshe.com/reaction/541306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
ReactantMethyl 4-(cyclobutylmethyl)-2-methylbenzoateHCID 68288684—
SolventAcetic AcidHCID 176—
ProductMethyl 4-(cyclobutylmethyl)-5-iodo-2-methylbenzoateHCID 6828897360.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a round-bottom flask was added a solution of methyl 4-(cyclobutylmethyl)-2-methylbenzoate (compound 189.1, 8.40 g, 38.5 mmol, 1.00 equiv) in AcOH (150 mL). NaIO4 (5.00 g, 23.4 mmol, 0.50 equiv), iodine (10.0 g, 39.4 mmol, 1.00 equiv), and sulfuric acid (0.3 mL) were added to the reaction mixture. The resulting solution was stirred at 60° C. for 12 h. After cooling to room temperature, the reaction was quenched with 200 mL of NaHSO3 (aq). The mixture was extracted with 2×200 mL of ethyl acetate, and the combined organic layers were dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified using silica gel column chromatography with ethyl acetate/petroleum ether (20:1) as eluent to furnish 8.00 g (60%) of methyl 4-(cyclobutylmethyl)-5-iodo-2-methylbenzoate as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08871790B2
Source datasetuspto-grants-2014_10
ORD IDord-693e0f6a088c4fef8909d68ac12ccfba
Source noteuspto-grants-2014_10