Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 482411Generated: October 25, 2026

Hydrochloric Acid → 2-(4-Isopropoxy-2-fluorophenyl)hydrazonomalonyldiurethane

https://huagongshe.com/reaction/482411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantCarbamic acid, (1,3-dioxo-1,3-propanediyl)bis-, diethyl esterHCID 154305—
ReactantSodium AcetateHCID 517045—
Reactant2-Fluoro-4-isopropoxyanilineHCID 3756384—
ReactantSodium NitriteHCID 23668193—
SolventWaterHCID 962—
Product2-(4-Isopropoxy-2-fluorophenyl)hydrazonomalonyldiurethaneHCID 6763057161.6%

Reaction Conditions

Temperature10 °C

Reaction Steps

A mixture of 5.92 g (0.035 mole) of 4-isopropoxy-2-fluoroaniline, 10.60 g (0.043 mole) of malonyldiurethane, and 41.02 g (0.500 mole) of sodium acetate was suspended in 1000 mL of water with vigorous stirring. To this suspension was added 25 mL of 12N hydrochloric acid. The reaction mixture was cooled to 10° C., and, while this temperature was maintained, a solution of 2.42 g (0.035 mole) of sodium nitrite in 25 mL of water was slowly added. The reaction mixture was allowed to warm slowly to room temperature where it was stirred under a nitrogen atmosphere for approximately 16 hours. During this period a yellow solid formed and precipitated out. The mixture was filtered, and the yellow solid was washed in succession with water and diethyl ether. After being dried, 9.20 g of 2-(4-isopropoxy-2-fluorophenyl)hydrazonomalonyldiurethane was isolated as a yellow solid. The NMR and IR spectra were consistent with the proposed structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05798316
Source datasetuspto-grants-1998_08
ORD IDord-835718db5e55486db5c593dfbf3f7d57
Source noteuspto-grants-1998_08