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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2691Generated: October 26, 2026

Imidazole → 2-(1-Imidazolyl)-1-phosphonoethanesulfonic acid

https://huagongshe.com/reaction/2691

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantWaterHCID 962—
ReactantBromotrimethylsilaneHCID 76113—
ReactantMethyl 1-dimethoxyphosphinylethenesulfonateHCID 18936079—
SolventChloroformHCID 6212—
Product2-(1-Imidazolyl)-1-phosphonoethanesulfonic acidHCID 18936076—

Reaction Steps

A mixture of 0.68 g (0.01 mole) of imidazole and 2.30 g (0.01 mole) of methyl 1-dimethoxyphosphinylethenesulfonate (U.S. Pat. No. 5,011,938 issued to Barnett et al. on Apr. 30, 1991) in 20 ml of chloroform is stirred at 20°-50° for one day. The reaction is cooled to room temperature, and 10.7 g (0.07 mole) of bromotrimethylsilane is added. The mixture is stirred at 20°-30° for 2-3 days, and to it is then added 20 ml water. The mixture is stirred for about 30 minutes, and the layers are separated. The water layer is extracted several times with CHCl3 (extracts are discarded) and is evaporated to dryness under vacuum. The residue is triturated with acetone to give a solid, which is collected by filtration and recrystallized from water/acetone to afford 2-(1-imidazolyl)-1-phosphonoethanesulfonic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05731299
Source datasetuspto-grants-1998_03
ORD IDord-b61bb71ca3fc444f88d24d728812b5de
Source noteuspto-grants-1998_03