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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 383134Generated: October 30, 2026

Imidazole → 4-Iodomethyl-2-(2-methylphenyl)benzoic acid, methyl ester

https://huagongshe.com/reaction/383134

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
Reactant4-Hydroxymethyl-2-(2-methylphenyl)benzoic acid methyl esterHCID 11391208—
SolventDiethyl EtherHCID 3283—
SolventAcetonitrileHCID 6342—
SolventDiethylether hexaneHCID 21584099—
Product4-Iodomethyl-2-(2-methylphenyl)benzoic acid, methyl esterHCID 2069991671.5%

Reaction Steps

Triphenylphosphine (5.16 g), and imidazole (1.34 g) were dissolved in 3:1 ether:acetonitrile (80 mL), and the reaction was cooled to 0° C. Iodine (5.0 g) was added with vigorous stirring, and the reaction was warmed to ambient temperature. After 1 h, the reaction was recooled to 0° C. and 4-hydroxymethyl-2-(2-methylphenyl)benzoic acid, methyl ester (example 1178C, 4.6 g) was added as a solution in ether (20 mL). After 4 h at ambient temperature, the reaction was diluted with hexane/ether (1:1, 200 mL) and filtered. The filtrate was washed with a dilute solution of Na2SO3 until colorless, then with water (2×50 mL). The organic extracts were washed with brine (20 mL), dried (MgSO4), filtered and concentrated. The residue was purified by silica gel chromatography eluting with 10% EtOAc/hexane to give a light yellow oil (4.7 g) which slowly crystalizes in the freezer.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06310095B1
Source datasetuspto-grants-2001_10
ORD IDord-7c95752e82e0463b9b91e422b2c52f22
Source noteuspto-grants-2001_10