Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 441709Generated: October 29, 2026

Oxygen → Ipronidazole-hydroxy

https://huagongshe.com/reaction/441709

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantPotassium HydroxideHCID 14797—
ReactantIpronidazoleHCID 26951—
ReactantTriethyl phosphiteHCID 31215—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
SolventHexamethylphosphoramideHCID 12679—
ProductIpronidazole-hydroxyHCID 59840221.6%

Reaction Steps

A total of 11.2 ml of triethylphosphite and 6 g of powdered potassium hydroxide were added to a solution of 8.5 g of 1-methyl-2-isopropyl-5-nitroimidazole in 40 ml of hexametapol while cooling in an ice-bath. While the solution was further cooled with ice, oxygen was conducted through the solution with vigorous stirring. After 2.5 hours, 6.1 ml of glacial acetic acid were added and the mixture was then poured into 600 ml of water and extracted four times with 150 ml portions of ether. The ether extracts were washed with a small amount of water, evaporated on a rotary evaporator and finally dried at 85°/0.5 Torr. The residue was crystallized from 15 ml of isopropyl ether. There were obtained 2.0 g of 2-(2-hydroxy-2-propyl)-1-methyl-5-nitroimidazole, melting point 102°-107°. The yield was 21.6%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04042597
Source datasetuspto-grants-1977_08
ORD IDord-fb3ffaff86e7458089a3b4ce9a58ed2f
Source noteuspto-grants-1977_08