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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609376Generated: October 26, 2026

Ammonia → HCID 10857978, compound

https://huagongshe.com/reaction/1609376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantSodium HydroxideHCID 14798—
Reactant4,6-DiaminoresorcinolHCID 458821—
Reactant1,2-Dichloro-3,5-dinitrobenzeneHCID 11020901—
ReactantCumen hydroperoxideHCID 53627471—
SolventDichloromethaneHCID 6344—
ProductHCID 10857978HCID 10857978—

Reaction Steps

In a preferred embodiment for making diaminoresorcinol, the base, e.g., sodium hydroxide, is first dissolved in refluxing liquid ammonia in an inert atmosphere. The temperature of refluxing liquid ammonia is dependent upon the pressure and is typically between about -50° C. to about -10° C. Under atmospheric pressure conditions, the refluxing temperature of liquid ammonia is about -33° C. A solution of cumene hydroperoxide and 1,2-dichloro-3,5-dinitrobenzene in methylene chloride is then added to the stirred liquid ammonia reaction mixture at a rate such that the temperature remains at the refluxing temperature. Upon completion of the addition, the ammonia is evaporated and 2,3-dichloro-4,6-dinitrophenol may be isolated by pouring the reaction mixture into excess aqueous hydrochloric acid and extracted with ethyl acetate. Preferably, the 2,3-dichloro-4,6-dinitrophenol product is not isolated or purified, but is directly converted to 4,6-diaminoresorcinol, thus making the production of 4,6-diaminoresorcinol from 1,2-dichloro-3,5-dinitrobenzene a "one pot" process.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399768
Source datasetuspto-grants-1995_03
ORD IDord-429a71b20f00411088209a83430522f2
Source noteuspto-grants-1995_03