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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230235Generated: October 26, 2026

Methyl iodide → Methyl 5-bromo-2-methylbenzoate

https://huagongshe.com/reaction/230235

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Bromo-2-methylbenzoic acidHCID 346004—
Reactant3-Bromo-2-methylbenzoic AcidHCID 2735590—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-bromo-2-methylbenzoateHCID 316201—

Reaction Steps

A 60:40 mixture of 5-bromo-2-methyl benzoic acid and 3-bromo-2-methyl benzoic acid (8.0 g, 0.037 mol) was dissolved in N,N′-dimethylformamide (130 mL). Methyl iodide (2.28 mL, 2.3 mol) and potassium carbonate (5.11 g, 0.037 mol) were added in sequence at room temperature. The mixture was stirred at room temperature for 2 hours at which point the reaction was determined to be complete by HPLC. The solvent was removed under high vacuum and the resulting residue was passed through a silica gel column using 5% ethyl acetate in hexanes as the eluent. The mixture of isomers was obtained as an oil and then separated by preparative normal phase HPLC using 0.5% isopropyl alcohol in hexanes as the eluent. The title compound was obtained as a white solid (1.38 g, 29%). 1H NMR (300.132 MHz, CDCl3) δ 8.04 (d, J=2.2 Hz, 1H), 7.50 (dd, J=8.2, 2.2 Hz, 1H), 7.12 (d, J=8.2 Hz, 1H), 3.89 (s, 3H), 2.54 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566727B2
Source datasetuspto-grants-2009_07
ORD IDord-7b151fd409a947519efff1a986c3af90
Source noteuspto-grants-2009_07