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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624307Generated: October 30, 2026

Iodine chloride → Methyl 5-iodo-2-methoxy-4-methylbenzoate

https://huagongshe.com/reaction/624307

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodine chlorideHCID 24640—
ReactantMethyl 2-methoxy-4-methylbenzoateHCID 7172021—
SolventMethanolHCID 887—
ProductMethyl 5-iodo-2-methoxy-4-methylbenzoateHCID 29934724—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of methyl 2-methoxy-4-methylbenzoate (2.6 g, 14.43 mmol) in methanol (25 ml) at room temperature in a 100 ml round bottomed (RB) flask was added iodine monochloride (3.62 ml, 72.1 mmol) in methanol dropwise. The reaction mixture was heated at 50° C. for 15 hours. The methanol was concentrated, diluted with water and extracted with ethyl acetate (3×25 ml). The combined organic extracts were washed with 0.1N HCl, water and brine solution. The organic layer was dried over Na2SO4, filtered and concentrated. The crude material was used for the next step without further purification (3.2 g, 73%). LCMS: (ES+) m/z=307 (M+H)+; Column: ZORBAX SB C18 (4.6×50) mm, 5 μm; Moblie (M) phase A: 10% MeOH-90% H2O-0.1% TFA; Moblie (M) phase B: 90% MeOH-10% H2O-0.1% TFA; Flow: 5 ml/min; Time (min.): 0 2 3; % B: 0 100 0; Retention Time (RT): 1.87 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303020B2
Source datasetuspto-grants-2016_04
ORD IDord-d31a8901faf243f2952617c723419f12
Source noteuspto-grants-2016_04