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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2372394Generated: October 25, 2026

Methane → 1-(2-Nitro-1-imidazolyl)-3-(3-bromopropylamino)-2-propanol hydrobromide

https://huagongshe.com/reaction/2372394

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantSodium HydroxideHCID 14798—
Reactant1-(2,3-Epoxypropyl)-2-nitroimidazoleHCID 334973—
Reactant3-Bromopropylazanium;bromideHCID 11031334—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product1-(2-Nitro-1-imidazolyl)-3-(3-bromopropylamino)-2-propanol hydrobromideHCID 14621567119.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution containing 3-bromopropylammonium bromide (6.47 g, 29.6 mmol) and sodium hydroxide (1.18 g, 29.5 mmol) in ethanol (40 cm3) was stirred at 20° C.; after 1 hour, diethyl ether (40 cm3) was added and the mixture filtered. 1-(2,3-epoxypropyl)-2-nitroimidazole (5.00 g, 29.6 mmol) was added to the filtrate and the solution heated to reflux for 45 minutes. The reaction mixture was then treated with decolourising charcoal (0.5 g), filtered, concentrated under reduced pressure and treated with aqueous hydrobromic acid (48% w/w HBr, 2.0 cm3). The solid which appeared upon refrigeration was recrystallised from aqueous ethanol to give 1-(2-nitro-1-imidazolyl)-3-(3-bromopropylamino)-2-propanol hydrobromide (6.87 g, 59.9%) as a hygroscopic yellow crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05098921
Source datasetuspto-grants-1992_03
ORD IDord-afdc90622a674874b9d06aa2d0a323fd
Source noteuspto-grants-1992_03