Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59800Generated: October 27, 2026

Methyl iodide → Methyl 3-iodo-4-methyl-5-nitrobenzoate

https://huagongshe.com/reaction/59800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Iodo-4-methyl-5-nitrobenzoic acidHCID 59627777—
SolventAcetoneHCID 180—
ProductMethyl 3-iodo-4-methyl-5-nitrobenzoateHCID 2472811098.3%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a solution of 3-iodo-4-methyl-5-nitro-benzoic acid (16.06 g, 52.3 mmol) in acetone (300 mL) was added K2CO3 (14.46 g, 104.6 mmol) followed by methyl iodide ((3.91 mL, 62.76 mmol). The reaction mixture was stirred at 40° C. overnight, then cooled to room temperature and partitioned between ethyl acetate and brine. The organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure to provide 16.5 g (98%) of 3-iodo-4-methyl-5-nitro-benzoic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440956B2
Source datasetuspto-grants-2016_09
ORD IDord-821743cb204d42a1a8a745aa8aed2a07
Source noteuspto-grants-2016_09