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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768441Generated: October 31, 2026

Nitrite → N-Nitrosodiphenylamine

https://huagongshe.com/reaction/1768441

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitriteHCID 946—
ReactantDiphenylamineHCID 11487—
ProductN-NitrosodiphenylamineHCID 6838—

Reaction Steps

diphenylamine method, where diphenylamine as raw material is nitrosated using a nitrite in an organic solvent to produce N-nitrosodiphenylamine, which is rearranged to 4-nitrosodiphenylamine hydrochloride under the action of anhydrous hydrogen chloride, and then, 4-nitrosodiphenylamine hydrochloride is neutralized with a base to give 4-nitrosodiphenylamine which is finally reduced to 4-aminodiphenylamine by sodium sulfide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07235694B2
Source datasetuspto-grants-2007_06
ORD IDord-199068b4def14006930f9d76383111a1
Source noteuspto-grants-2007_06