Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1580125Generated: October 26, 2026

Hydrochloric Acid → 1-(2-Hydroxy-5-nitrobenzyl)-2-imidazolidinone

https://huagongshe.com/reaction/1580125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium IodideHCID 4875—
Reactant2-ImidazolidinoneHCID 8453—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Hydroxy-5-nitrobenzyl bromideHCID 13044—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
Product1-(2-Hydroxy-5-nitrobenzyl)-2-imidazolidinoneHCID 13006892—

Reaction Steps

A 7.9 g (0.092 mole) portion of 2-imidazolidinone in 92 ml of dimethylsulfoxide was treated with 12.7 g (0.092 mole) of K2CO3, 7.4 g (0.045 mole) of potassium iodide and 20.0 g (0.092 mole) of 2-hydroxy-5-nitrobenzyl bromide. The reaction mixture was heated to 105° over 0.3 hours and held at 105° for 1.6 hours. The reaction mixture was poured with stirring into 550 ml of water. The aqueous mixture was acidified with 9 ml of concentrated HCl and extracted with 480 ml of chloroform. The chloroform extract was washed with 60 ml of H2O, dried over MgSO4 overnight and filtered. The filtrate was concentrated under reduced pressure to give 18 g of a yellow semi-solid. The crude product was crystallized using 65 ml of benzene and filtered, washing with ether to give 9.7 g (44%) of a light yellow semi-solid. Recrystallization from acetonitrile gave an analytical sample, m.p. 222°-224° dec.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03932452
Source datasetuspto-grants-1976_01
ORD IDord-68b133b975dd448389ab1c8fc39c6058
Source noteuspto-grants-1976_01