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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1756597Generated: October 27, 2026

Hydrogen Peroxide → HCID 178440202, compound

https://huagongshe.com/reaction/1756597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen PeroxideHCID 784—
ReactantTriethylamineHCID 8471—
ReactantButyryl chlorideHCID 8855—
ReactantSodium HydroxideHCID 14798—
Reactant2-Amino-5-nitrobenzonitrileHCID 28532—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178440202HCID 178440202—

Reaction Steps

To a solution of 16.3 g (0.1 mol) of 2-amino-5-nitrobenzonitrile in 200 ml of CH2Cl2 at 0° C. was added 21 ml (0.15 mol) of triethyl amine followed by 0.3 g of DMAP and 11.71 g (0.11 mol) of butyryl chloride. The reaction mixture was warmed to room temperature and then heated over night at 50° C. The solution was washed with 1N HCl (1×20 ml), water (1×20 ml), saturated NaHCO3 (2×20 ml) and brine (1×20 ml) and dried over MgSO4. The solution was filtered and concentrated in vacuo. The residue was dissolved in 200 ml of MeOH to which was added 44 ml (0.22 mol) of 5M NaOH solution followed by the dropwise addition of 25 ml (0.22 mol) 30% H2O2 and 50 ml of water. The mixture was refuxed for 4 hours, cooled and filtered. The filtrate was acidified with 1N HCl and the resulting precipitate recovered by filtration. The residue was recrystalized from MeOH to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05441959
Source datasetuspto-grants-1995_08
ORD IDord-f0dbef264bea4498846b7673aef8d9dc
Source noteuspto-grants-1995_08