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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337659Generated: October 28, 2026

Imidazole → Methyl 3-bromo-5-(iodomethyl)-4-methylbenzoate

https://huagongshe.com/reaction/337659

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantIodineHCID 807—
ReactantTriphenylphosphineHCID 11776—
ReactantMethyl 3-bromo-5-(hydroxymethyl)-4-methylbenzoateHCID 66896191—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-bromo-5-(iodomethyl)-4-methylbenzoateHCID 66896553—

Reaction Steps

To a dichloromethane (0.05 M) solution of triphenylphosphine (1.1 eq) was added iodine (1.1 eq.). The resulting orange-yellow suspension was stirred at RT for 30 min before imidazole (1.2 eq.) and finally methyl 3-bromo-5-(hydroxymethyl)-4-methylbenzoate (1 eq.) from the previous step were added. The now pale yellow solution was stirred at RT for another 30 min. The volatiles were removed in vacuo and the residue was triturated with a 1:1 (v/v) mixture of hexanes and ether. The insolubles were then removed via filtration through a pad of silica gel. Concentration of the filtrate in vacuo afforded the title compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889714B2
Source datasetuspto-grants-2014_11
ORD IDord-2abfda4e64324c5b9869a32e5436db68
Source noteuspto-grants-2014_11