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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227359Generated: October 29, 2026

Methyl iodide → Methyl 5-iodo-2-methoxybenzoate

https://huagongshe.com/reaction/227359

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantEthyl AcetateHCID 8857—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Iodo-2-methoxybenzoateHCID 21094541—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-iodo-2-methoxybenzoateHCID 1101176288%

Reaction Steps

Methyl iodide (2.40 mL, 38.48 mmol) and K2CO3 (10.60 g, 76.96 mmol) were added to a solution of 5-iodo-2-methoxybenzoate (5.37 g, 19.24 mmol) in DMF (20 mL) and stirred at rt under Ar for 24 h. Upon completion, ethyl acetate was added and the reaction was washed with 1% HCl (2×20 mL), brine (1×), dried over MgSO4 and concentrated in vacuo. The residue was purified by flash chromatography (3:1 hexane:ethyl acetate) to afford methyl-5-iodo-2-methoxybenzoate (4.93 g, 88%) as a white solid. See, for example, Corey, E. J.; Myers, A. G. J. Am. Chem. Soc. 1985, 107, 5574-5576, which is incorporated by reference in its entirety. 1H NMR (DMSO-d6, 400 MHz) δ 7.90 (d, 1H, J=2.4 Hz), 7.80 (dd, 1H, J=8.8, 2.4 Hz), 6.96 (d, 1H, J=9.0 Hz), 3.81 (s, 3H), 3.79 (s, 3H). 13C NMR (DMSO-d6, 100 MHz) δ 164.7, 158.0, 141.6, 138.5, 122.2, 115.2, 82.1, 55.9, 52.0. HREIMS calculated for C9H9IO3 (M+) 291.9608. found 291.9596.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560488B2
Source datasetuspto-grants-2009_07
ORD IDord-87edd9cf2b164e0e9fd96fe732bc5999
Source noteuspto-grants-2009_07